NDC 51672-4060-01 - Amcinonide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 51672-4060
Requested NDC: 51672-4060-01
Package NDCs from labels: 51672-4060-1, 51672-4060-2, 51672-4060-3, 51672-4060-01
Manufacturer: Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
Effective date: 2025-04-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Amcinonide Cream USP, 0.1% Amcinonide Ointment USP, 0.1%	Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries Ltd.	2025-04-03	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-4060-1	Amcinonide	1 in 1 CARTON	OINTMENT	1	5
51672-4060-1	Amcinonide	15 g in 1 TUBE	OINTMENT	15	5
51672-4060-2	Amcinonide	30 g in 1 TUBE	OINTMENT	30	5
51672-4060-2	Amcinonide	1 in 1 CARTON	OINTMENT	1	5
51672-4060-3	Amcinonide	1 in 1 CARTON	OINTMENT	1	5
51672-4060-3	Amcinonide	60 g in 1 TUBE	OINTMENT	60	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-4060	AMCINONIDE CREAM AMCINONIDE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.]	5	Current NDC, Legacy NDC, 6 package rows	20250406_ac5c3e79-52f7-434e-92ae-24bd32b45edc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Amcinonide	ACTIVE INGREDIENT	423W026MA9	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
Amcinonide	ACTIVE MOIETY	423W026MA9	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
anhydrous citric acid	INACTIVE INGREDIENT	XF417D3PSL	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
butylated hydroxyanisole	INACTIVE INGREDIENT	REK4960K2U	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
isopropyl palmitate	INACTIVE INGREDIENT	8CRQ2TH63M	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
lactic acid	INACTIVE INGREDIENT	33X04XA5AT	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
petrolatum	INACTIVE INGREDIENT	4T6H12BN9U	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
propyl gallate	INACTIVE INGREDIENT	8D4SNN7V92	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
propylene glycol	INACTIVE INGREDIENT	6DC9Q167V3	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
sorbitol	INACTIVE INGREDIENT	506T60A25R	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2
water	INACTIVE INGREDIENT	059QF0KO0R	AMCINONIDE CREAM AMCINONIDE OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]	2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 57 of 57 · 1,123 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Health Original SPF 15 Lip Balm	OXYBENZONE, OCTINOXATE, PETROLATUM	CVS	e49680bd-bd61-40cf-abc8-51a1c8808726	2016-09-14	Warnings	Exact identifier unii: 4T6H12BN9U
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.