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A01010 Summary:

BILL NOA01010B
 
SAME ASSAME AS S08880-A
 
SPONSORWeprin
 
COSPNSR
 
MLTSPNSR
 
Amd Art 38-A Art Head, 820, Gen Bus L
 
Makes it illegal to knowingly alter, mutilate, destroy, obliterate, obstruct or remove by means of a price sticker or otherwise the whole or any part of the label, including where applicable the expiration date displayed thereon, of any over-the-counter drug or cosmetic.
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A01010 Actions:

BILL NOA01010B
 
01/13/2023referred to consumer affairs and protection
05/16/2023reported referred to rules
01/03/2024referred to consumer affairs and protection
02/27/2024reported referred to codes
03/07/2024amend (t) and recommit to codes
03/07/2024print number 1010a
04/04/2024amend and recommit to codes
04/04/2024print number 1010b
04/09/2024reported
04/12/2024advanced to third reading cal.400
04/15/2024passed assembly
04/15/2024delivered to senate
04/15/2024REFERRED TO CONSUMER PROTECTION
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A01010 Memo:

NEW YORK STATE ASSEMBLY
MEMORANDUM IN SUPPORT OF LEGISLATION
submitted in accordance with Assembly Rule III, Sec 1(f)
 
BILL NUMBER: A1010B
 
SPONSOR: Weprin
  TITLE OF BILL: An act to amend the general business law, in relation to the sale of over-the-counter drugs and cosmetic products   PURPOSE: To promote and protect the health and safety of purchasers of O-T-C drugs and cosmetics by enabling them to read such products' packaging or labels in a complete, unaltered and unobstructed condition, at the time of purchase or thereafter. Such labels are required by federal law and regulations.   SUMMARY OF PROVISIONS: Section 1. Changes the article heading of Article 38-A of the General Business law. Section 2. Amends subdivisions 1 and 2 of Section 820 of the General Business law, to make it unlawful for any retailer to knowingly alter, obstruct, obscure or remove, by means of a sticker, tag or other device used to deter theft, or a price sticker, or otherwise, the whole or any part of the label or packaging of any over-the-counter (0-T-C) drug or cosmetic as such label is required by the federal Food, Drug and Cosmet- ic Art, and by the Food and Drug Administration's (FDA) rules and regu- lations that implement the Act's label requirements for such products. Violators would be subject to the existing enforcement remedy contained in GBL, Section 821. Under that provision, compliance with FDA rules and regulations constitutes a complete defense to any enforcement action. Also adds a new subdivision 3 to the section providing definitions for label and cosmetic.   JUSTIFICATION: At the very foundation of consumer protection for purchasers of 0-T-C drugs and cosmetics are the labeling requirements of Chapters V and VI of the Federal Food, Drug and Cosmetic Act and the implementing regu- lations of the Food and Drug Administration. (See 21 C.F.R. Part 201, Subchapter C, et seq. (0-T-C drugs) and 21 FR Part 701 cosmetics). Drug labels provide vital health and safety information including indi- cations, directions for use, warnings and precautions, drug interaction information, cautions and list of ingredients. Cosmetic labels must contain a designation of ingredients, a requirement of special impor- tance for users who suffer particular allergic reactions. In early 1920, the Department of Law's Bureau of Consumer Frauds and Protection conducted a random survey of drug stores operated by eight major chains located in the metropolitan New York City area in an effort to determine whether the labels of O-T-C drugs or cosmetics offered for sale to the public were being obscured or obstructed by the retailers' practice of superimposing upon such labels the store's own price stick- ers or security stickers or other devices intended to deter theft. The survey revealed that in a significant number of instances, retailers were obstructing or obscuring product labels by placing paper stickers or plastic devices over the manufacturer's product labels. This practice made it impossible, in many cases, for prospective purchasers to read the labels before purchase. Even after purchase, consumers, in many cases, would be unable to read the labels because the removal of the retailer's stickers would result in the unintended destruction of the manufacturer's label as well. Indeed, in one case, the cashier at a major drug retail chain store tore off the store's sticker from the principal display panel of an O-T-C drug product and, in doing so, destroyed the manufacturer's label at the same time. In general, this practice could have severe health and safety consequences. For example, the product in question in this particular case was "Colly rium Fresh Sterile Eye Drops" manufactured by Wyeth Laboratories. That part of the manufacturer's label destroyed by the store's cashier included crucial product warnings and cautions, as follows: Warnings: Do not use if solution changes color or becomes cloudy. Remove contact lenses before using if you have glaucoma do not use this product except under the advice and supervision of a physician. Overuse of this product may produce increased redness of the eye. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. If you experience eye pain, changes in vision, contin- ued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a physi- cian. Keep this and all medication out of the reach of children. Retain this carton for complete product information. Keep bottle lightly closed at Room Temperature; Approx. 77 degrees F/25 degrees C. The Department of Law survey confirmed that the above-described practice by retail drug stores is common and widespread. Case by case enforcement would not offer consumers the full protection that a legislative initi- ative offers. This bill builds upon an earlier law that addressed a related problem. In 1985, a survey published by the Department of Law revealed, inter aide, that retailers of O-T-C drugs were similarly obstructing the expiration date of such drug products offered for sale. (See Expiration. Dating of Over-TheCounter Drugs in New York, a report by New York State Attorney General Robert Abrams (January 1985)). Subse- quently, the Legislature adopted an Attorney General's Program bill (1986, Ch. 697) that included GBL Section 820(2), a provision that makes such practice unlawful. The present proposal would offer parallel protection for consumers with regard to the obstruction of labels.   LEGISLATIVE HISTORY: 2023: referred to rules 2021/2022: referred to consumer affairs and protection 2019/2020: referred to consumer affairs and protection 2017/2018: referred to consumer affairs and protection   FISCAL IMPLICATIONS: None.   EFFECTIVE DATE: This act shall take effect immediately.
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A01010 Text:



 
                STATE OF NEW YORK
        ________________________________________________________________________
 
                                         1010--B
 
                               2023-2024 Regular Sessions
 
                   IN ASSEMBLY
 
                                    January 13, 2023
                                       ___________
 
        Introduced by M. of A. WEPRIN -- read once and referred to the Committee
          on  Consumer Affairs and Protection -- recommitted to the Committee on
          Consumer Protection in accordance with Assembly  Rule  3,  sec.  2  --
          reported   and  referred  to  the  Committee  on  Codes  --  committee
          discharged, bill amended, ordered reprinted as amended and recommitted
          to said committee -- again reported from said  committee  with  amend-
          ments, ordered reprinted as amended and recommitted to said committee
 
        AN  ACT  to  amend  the general business law, in relation to the sale of
          over-the-counter drugs and cosmetic products
 
          The People of the State of New York, represented in Senate and  Assem-
        bly, do enact as follows:
 
     1    Section 1. The article heading of article 38-A of the general business
     2  law,  as added by chapter 697 of the laws of 1986, is amended to read as
     3  follows:
     4                               SALE OF OUTDATED
     5               AND LABEL OBSTRUCTED OVER-THE-COUNTER DRUGS AND
     6                              COSMETIC PRODUCTS
     7    § 2. Section 820 of the general business law, as added by chapter  697
     8  of the laws of 1986, is amended to read as follows:
     9    § 820. Unlawful practices. 1. It shall be unlawful for any retailer:
    10    [1.]  (a)  to  knowingly  sell or offer for sale, any drug or cosmetic
    11  sold over-the-counter without the need of a prescription, later than the
    12  date, if any, marked upon the label as indicative  of  the  date  beyond
    13  which the contents cannot be expected beyond reasonable doubt to be safe
    14  and  effective;  provided,  however,  that when such drug or cosmetic is
    15  identified as an outdated drug or cosmetic by segregation  from  regular
    16  stock or by other means, the holding of such drug or cosmetic beyond its
    17  expiration  date  shall  not be deemed a violation of this section. When
    18  the expiration date is expressed by month and year, the expiration  date
    19  shall be the last day of the month indicated; or

         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD01243-04-4

        A. 1010--B                          2
 
     1    [2.]  (b)  to knowingly alter, mutilate, destroy, obliterate, obstruct
     2  or remove by means of a price sticker or otherwise the whole or any part
     3  of [the expiration date displayed on] the label or packaging, including,
     4  where applicable, the expiration date displayed thereon,  of  any  over-
     5  the-counter drug or cosmetic.
     6    2.  For  purposes  of this section, the following terms shall have the
     7  following meanings:
     8    (a) "label" shall mean the label required by the  statutes  applicable
     9  to  and  regulations issued by the federal food and drug administration;
    10  and
    11    (b) "cosmetic" shall mean   articles   intended    to    be    rubbed,
    12  poured,  sprinkled  or sprayed on, introduced into, or otherwise applied
    13  to the human body or any part thereof   for   cleansing,    beautifying,
    14  promoting  attractiveness, or altering the appearance, including but not
    15  limited to personal hygiene  products  such  as  deodorant,  shampoo  or
    16  conditioner.
    17    § 3. This act shall take effect immediately.
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