Home NDC 76348-413 Margarite Zinc Cream
Product NDC 76348-413
11-digit product format 763480413
Labeler code 76348
Product ID 76348-413_373b8aa5-564e-3e75-e063-6394a90af372
Type HUMAN OTC DRUG
Nonproprietary name Zinc Cream
Dosage form CREAM
Route TOPICAL
Labeler Renu Laboratories, LLC
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-10-13
Substance SULFUR
Active strength 1.12 g/28g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 76348-413-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 76348-413-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 76348-413-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 76348-413-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76348-413-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76348-413-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76348-413-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Margarite Zinc Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 1.12 g/28g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 247817 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# 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 6 of 56 · 1,101 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join GlowBiotic Probiotic Acne Cleanser SALICYLIC ACID Glowbiotics 546334bf-cf47-a1e5-e063-6394a90a590c 2026-06-16 Warnings Exact identifier application number: M006 La Roche Posay Laboratoire Dermatologique Effaclar Duo Plus M MultiTarget Acne Treatment SALICYLIC ACID L'Oreal USA Products Inc 5464d48b-495c-e45f-e063-6394a90aedfc 2026-06-16 Warnings Exact identifier application number: M006 La Roche Posay Laboratoire Dermatologique Effaclar Duo Plus M MultiTarget Acne Treatment SALICYLIC ACID COSMETIQUE ACTIVE PRODUCTION 54650326-1582-26b7-e063-6394a90a575c 2026-06-16 Warnings Exact identifier application number: M006 Butterflys tear MILIA REMOVER SALICYLIC ACID 1% MILIA REMOVER Jiangxi Yudexi Pharmaceutical Co., LTD 52226dfd-eafa-42d7-e063-6394a90a16ef 2026-06-12 Warnings Exact identifier application number: M006 Proven Acne Cleanser SALICYLIC ACID Proven Skincare 316702b8-4f9d-0a42-e063-6394a90ad8e1 2026-06-11 Warnings Exact identifier application number: M006 Proven Acne Cleanser SALICYLIC ACID Proven Skincare 31a29bdd-a218-247a-e063-6294a90a8cee 2026-06-11 Warnings Exact identifier application number: M006 Clopoat CLOPOAT ACNE-CLEARING SPOT COLLOIDAL SULFUR Guangzhou Meixi Biotechnology Co., Ltd. 53cd1d6b-d44c-2508-e063-6294a90a96c6 2026-06-09 Warnings Exact identifier application number: M006 Good Molecules Acne Foaming Cleanser SALICYLIC ACID Twincraft Inc. 4911ef14-b465-3398-e063-6394a90a9c9a 2026-06-09 Warnings Exact identifier application number: M006 PanOxyl Pore Refining Acne Mask SULFUR Crown Laboratories, Inc. 5373574c-95be-dd88-e063-6394a90ae519 2026-06-05 Warnings Exact identifier application number: M006 Acne Control Serum BENZOYL PEROXIDE Private Label Skin Care d4a4b89f-c9cf-4188-9c61-e8ef22b7638c 2026-06-03 Warnings Exact identifier application number: M006 BellamiLuxx Body acne cleanser BENZOYL PEROXIDE 4% BellamiLuxx LLC 532baae0-7e6f-1764-e063-6394a90a11ce 2026-06-01 Warnings Exact identifier application number: M006 Clean and Clear Acne Spot Treatment SALICYLIC ACID Kenvue Brands LLC 532c48d7-6d7b-ba96-e063-6394a90a9c30 2026-06-01 Warnings Exact identifier application number: M006 SkinCeuticals Blemish Plus Age Defense Acne Treatment SALICYLIC ACID LOreal USA Products Inc 727fa830-1f71-40ae-8153-7a29dbcb5e29 2026-06-01 Warnings Exact identifier application number: M006 Hero Pore Release Blackhead Clearing SALICYLIC ACID Church & Dwight Co., Inc. 436cf03c-3f74-4a02-bb0a-1d24f5c4fc29 2026-06-01 Warnings Exact identifier application number: M006 Principal Secret Blemish Buster Clear SALICYLIC ACID Guthy-Renker LLC 75387738-eca2-4184-833b-95005eb27666 2026-05-29 Warnings Exact identifier application number: M006 KUGIG ACNE TREATMENT SPRAYER SALICYLIC ACID Guangdong Jiaoyu Biotechnology Co., Ltd. 52b1e9cb-c083-a6eb-e063-6294a90ab6d1 2026-05-26 Warnings Exact identifier application number: M006 LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE BENZOYL PEROXIDE EFFACLAR BPO BENZOYL PEROXIDE LOreal USA Products Inc 851882ac-56f4-4bf6-b942-6efea10eec3e 2026-05-26 Warnings Exact identifier application number: M006 BLEMISH DOTS - RETINOL (10 PATCHES) SALICYLIC ACID 0.5% MELON BIO-TECH (THAILAND) CO., LTD. 201eeecd-e759-42b8-b5c2-b19465d98332 2026-05-25 Warnings Exact identifier application number: M006 BLEMISH DOTS - CHARCOAL (10 PATCHES) SALICYLIC ACID 0.5% MELON BIO-TECH (THAILAND) CO., LTD. a5431ecd-0afc-4525-9157-ee05ff752df5 2026-05-25 Warnings Exact identifier application number: M006 XEXLVOV MILIA REMOVER SALICYLIC ACID 1% MILIA REMOVER LIQUID Shanghai Honghui Chuang Intelligent Technology Co., Ltd 529bf32f-b40b-9602-e063-6294a90a1c2a 2026-05-24 Warnings Exact identifier application number: M006
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76348-413-01 76348041301 28 g in 1 TUBE 28 g Historical 76348-413-02 76348041302 1 TUBE in 1 BOX (76348-413-02) / 28 g in 1 TUBE (76348-413-01) 1 tube 2015-10-13 0000-00-00 No No Current