Isopropyl Rubbing Alcohol Wintergreen

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	71927-026		I	Inactivated by FDA		2026-08-07
excluded package	package	71927-026	71927-026-01	I	Inactivated by FDA		2026-08-07

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71927-026-01	Isopropyl Rubbing Alcohol WintergreenOrazen Inc	354 mL in 1 BOTTLE, PLASTIC	LIQUID	354		1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
ND2M416302	ISOPROPYL ALCOHOL	67-63-0	ISOPROPYL ALCOHOL

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
616456	isopropyl alcohol 50 % Topical Solution	PSN	3716cdac-1770-5e53-e063-6294a90a7849	1
616456	isopropyl alcohol 0.5 ML/ML Topical Solution	SCD	3716cdac-1770-5e53-e063-6294a90a7849	1
616456	isopropyl alcohol 50 % Topical Solution	SY	3716cdac-1770-5e53-e063-6294a90a7849	1

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
71927-026-01	71927002601	354 mL in 1 BOTTLE, PLASTIC (71927-026-01)	354 ml	2025-06-02	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Isopropyl Rubbing Alcohol, 50% Wintergreen Orazen Inc. Our Brand	Orazen Inc \| Onest Ltd	2025-06-08	HUMAN OTC DRUG LABEL	1