NDC 76348-413-01 - Margarite Zinc Cream

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: 76348-413
Requested NDC: 76348-413-01
Package NDCs from labels: 76348-413-01, 76348-413-02
Manufacturer: Renu Laboratories, LLC
Effective date: 2025-06-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Margarite Zinc Cream - Renu Laboratories, LLC	Renu Laboratories, LLC	2025-06-10	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76348-413-02	2025-06-10	C162847	48780-1	2cef2736-5b8b-d83d-e063-dadaa90ab31f	MARGARITE ZINC CREAM
76348-413-02	2025-01-30	C162847	48780-1	2cef2736-5b8b-d83d-e063-dadaa90ab31f	MARGARITE ZINC CREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76348-413-01	Margarite Zinc Cream	28 g in 1 TUBE	CREAM	28		11
76348-413-02	Margarite Zinc Cream	1 in 1 BOX	CREAM	1		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76348-413	MARGARITE ZINC CREAM (ZINC CREAM) CREAM [RENU LABORATORIES, INC.]	10	Current NDC, Legacy NDC, 2 package rows	20220115_3ca3b7d8-702a-036b-e054-00144ff8d46c.zip

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 324 of 324 · 6,465 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens Zinc SPF 50	OCTOCRYLENE, ZINC OXIDE	Walgreens	c71f4460-a316-428b-9a87-50c41065bc5b	2016-01-05	Warnings	Exact identifier unii: SOI2LOH54Z
TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted)	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	6a996e03-907f-4e6a-b232-0892b86956b0	2015-08-21	Warnings	Exact identifier unii: SOI2LOH54Z unii: 15FIX9V2JP
Renewal Firming Day Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	BURT'S BEES, INC.	18ceb5d8-4b76-6a54-e054-00144ff88e88	2015-06-18	Warnings	Exact identifier unii: SOI2LOH54Z unii: 15FIX9V2JP
SKIN MEDICA Purifying Foaming Wash	SALICYLIC ACID	Allergan, Inc.	064d9e2b-077f-4229-b653-666fc5479ae2	2013-03-01	Warnings	Exact identifier application number: M006
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD.	30468afc-9616-4765-b046-12e97a0a7827	2010-12-20	Warnings	Exact identifier unii: SOI2LOH54Z unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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