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HB4392 • 2026

Banning certain dyes from pharmaceutical products

Banning certain dyes from pharmaceutical products

Passed Legislature

This bill passed both chambers and reached final enrollment, even if later executive action is not shown here.

Sponsor
Burkhammer
Last action
2026-02-03
Official status
H Markup Discussion 02/03/26
Effective date
Not listed

Plain English Breakdown

The plain English breakdown is still being put together. The official documents below are already here.

Bill History

  1. 2026-02-03 H

    Markup Discussion

  2. 2026-01-15 H

    To House Health and Human Resources

  3. 2026-01-15 H

    Introduced in House

  4. 2026-01-15 H

    To Health and Human Resources

  5. 2026-01-15 H

    Filed for introduction

Official Summary Text

Banning certain dyes from pharmaceutical products

Current Bill Text

Read the full stored bill text
HB 4392 Text

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Introduced Version

House Bill 4392 History

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WEST VIRGINIA LEGISLATURE
2026
REGULAR SESSION
Introduced
House Bill 4392
By Delegate Burkhammer
[Introduced January 15, 2026; referred to the Committee on Health and Human Resources]
A BILL to amend and reenact §16-7-2 of the Code of West Virginia,1931, as amended, relating to adulteration of pharmaceutical products; and banning certain dyes from pharmaceutical products.
Be it enacted by the Legislature of West Virginia:

ARTICLE 7. PURE FOOD AND DRUGS.

§16-7-2. What constitutes adulteration.

Any drug or article of food shall be deemed to be adulterated within the meaning of this article: for the purpose of this article:
(a) In the case of drugs:
(1) If, when sold under or by a name recognized in the United States Pharmacopoeia official at that time, it differs from the standard of strength, quality, or purity laid down therein;
(2) If, when sold under or by a name not recognized in the United States Pharmacopoeia official at the time, but which is found in some other pharmacopoeia or other standard work of materia medica, it differs materially from the standard of strength, quality, or purity laid down in such work;
(3) If its strength, quality, or purity falls below the professed standard under which it is sold;
(4) If it be an imitation of, or offered for sale under the name of, another article;
or
(5) If the contents of the package as originally put up shall have been removed in whole or in part, and other contents shall have been placed in such package, or if the package fails to bear a statement on the label of the quantity or proportion of any alcohol, morphine, opium, cocaine, heroin, alpha or beta eucaine, chloroform, cannabis indicia, chloral hydrate, acetanilide, or any derivative or preparation of any such substance contained therein:
Provided
, That nothing in this paragraph shall be construed to apply to the dispensing of prescriptions written by regular licensed practicing physicians, veterinary surgeons, or dentists, and kept on file by the dispensing pharmacist, nor to such drugs as are recognized in the United States Pharmacopoeia and the National Formulary, which are sold under the name by which they are recognized
.

;or
(6) If it contains any added substance or ingredients which are poisonous or injurious to the health, including FD&C Blue No. 1, FD&C Blue No. 2, FD&C Green No. 3, FD&C Red No. 3, FD&C Red No. 40, FD&C Yellow No. 5, and FD&C Yellow No. 6.
(b) In the case of food, drink, confectionery, or condiment:
(1) If any substance or substances have been mixed with it, so as to lower or depreciate or injuriously affect its quality, strength, or purity;
(2) If any inferior or cheaper substance or substances have been substituted wholly or in part for it;
(3) If any valuable or necessary constituent or ingredient has been wholly or in part abstracted from it;
(4) If it is an imitation of, or is sold under the name of, another article;
(5) If it consists wholly or in part of diseased, decomposed, putrid, infected, tainted, or rotten animal or vegetable substance, whether manufactured or not, or, in the case of milk, if it is the product of a diseased animal;
(6) If it is colored, coated, polished, or powdered, whereby damage or inferiority is concealed, or if by any means it is made to appear better or of greater value than it really is;
(7) If it contains any added substance or ingredients which are poisonous or injurious to the health, including butylated hydroxyanisole, propylparaben, FD&C Blue No. 1, FD&C Blue No. 2, FD&C Green No. 3, FD&C Red No. 3, FD&C Red No. 40, FD&C Yellow No. 5, and FD&C Yellow No. 6;
(8) If it is sold under a coined name and does not contain some ingredient suggested by such name or contains only an inconsiderable quantity; or
(9) If the package containing it or any label thereon shall bear any statement regarding it or its composition which shall be false or misleading in any particular:
Provided
, That the provisions of this article do not apply to mixtures or compounds recognized as ordinary articles or ingredients of articles of food or drink, if each and every package sold or offered for sale is distinctly labeled in words of the English language as mixtures or compounds, with the name and percent of each ingredient therein; the word "compound" or "mixture" shall be printed in type not smaller in either height or width than one half the largest type upon any label on the package, and the formula shall be printed in letters not smaller in either height or width than one fourth the largest type upon any label on the package, and said compound or mixture must not contain any ingredients injurious to the health.
(10)

(c)
The amendments made to this section during the 2025 regular session of the Legislature shall be effective on January 1, 2028
;

.

NOTE: The purpose of this bill is to ban certain dyes from pharmaceutical products.
Strike-throughs indicate language that would be stricken from a heading or the present law and underscoring indicates new language that would be added.

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