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Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment.
Fed Regist. 2000 Jan 03; 65(1):7-9.FR

Abstract

The Food and Drug Administration (FDA) is amending the regulation that established a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products, and is amending several related OTC drug product labeling regulations. This amendment corrects and conforms several aspects of the new labeling requirements to other regulatory provisions and eliminates unnecessary text from the new labeling regulation.

MeSH

Consumer Product SafetyDrug LabelingHumansLegislation, DrugNonprescription DrugsUnited StatesUnited States Food and Drug Administration

Pub Type(s)

Journal Article

Language

eng

PubMed ID

11010625

Citation

"Over-the-counter Human Drugs; Labeling Requirements; Final Rule; Technical Amendment. Food and Drug Administration, HHS. Final Rule; Technical Amendment." Federal Register, vol. 65, no. 1, 2000, pp. 7-9.
Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment. Fed Regist. 2000;65(1):7-9.
(2000). Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment. Federal Register, 65(1), 7-9.
Over-the-counter Human Drugs; Labeling Requirements; Final Rule; Technical Amendment. Food and Drug Administration, HHS. Final Rule; Technical Amendment. Fed Regist. 2000 Jan 3;65(1):7-9. PubMed PMID: 11010625.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment. PY - 2000/9/30/pubmed PY - 2000/9/30/medline PY - 2000/9/30/entrez SP - 7 EP - 9 JF - Federal register JO - Fed Regist VL - 65 IS - 1 N2 - The Food and Drug Administration (FDA) is amending the regulation that established a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products, and is amending several related OTC drug product labeling regulations. This amendment corrects and conforms several aspects of the new labeling requirements to other regulatory provisions and eliminates unnecessary text from the new labeling regulation. SN - 0097-6326 UR - https://www.unboundmedicine.com/medline/citation/11010625/Over_the_counter_human_drugs DB - PRIME DP - Unbound Medicine ER -

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