Home NDC 69148-001 ARC Skin Protectant
Product NDC 69148-001
11-digit product format 691480001
Labeler code 69148
Product ID 69148-001_8b450573-d048-4077-8c0b-9e0a2e8a72c2
Type HUMAN OTC DRUG
Nonproprietary name ALLANTOIN
Dosage form OINTMENT
Route TOPICAL
Labeler Anjon Biologics, Inc
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-08-06
Substance ALLANTOIN
Active strength .5 g/100g
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 · 15 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69148-001-00 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 69148-001-00 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 69148-001-00 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 69148-001-00 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 69148-001-00 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 69148-001-00 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 69148-001-00 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 69148-001-00 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69148-001-00 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 69148-001-00 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 69148-001-00 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 69148-001-00 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69148-001-00 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69148-001-01 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…
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 ARC Skin Protectant
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN .5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1044541 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 69148-001-00 ARC Skin Protectant 118.6 g in 1 TUBE OINTMENT 118.6 6 69148-001-01 ARC Skin Protectant 60 g in 1 TUBE OINTMENT 60 6 69148-001-02 ARC Skin Protectant 100 g in 1 TUBE OINTMENT 100 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALLANTOIN ACTIVE INGREDIENT 344S277G0Z ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 ALLANTOIN ACTIVE MOIETY 344S277G0Z ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 BENZOIC ACID INACTIVE INGREDIENT 8SKN0B0MIM ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 COCONUT OIL INACTIVE INGREDIENT Q9L0O73W7L ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 IMIDUREA INACTIVE INGREDIENT M629807ATL ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 JOJOBA OIL INACTIVE INGREDIENT 724GKU717M ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 METHYLISOTHIAZOLINONE INACTIVE INGREDIENT 229D0E1QFA ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 SHEA BUTTER INACTIVE INGREDIENT K49155WL9Y ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 SORBITAN TRISTEARATE INACTIVE INGREDIENT 6LUM696811 ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 VITAMIN A INACTIVE INGREDIENT 81G40H8B0T ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69148-001 ARC SKIN PROTECTANT (ALLANTOIN) OINTMENT [ANJON BIOLOGICS, INC] 6 Current NDC, Legacy NDC, 3 package rows 20240426_f4ff79dd-cb38-4cca-9631-a2758a171873.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 36 of 68 · 1,357 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join JAFRA Fruteria Coco Fresco Lip Balm DIMETHICONE Distribuidora Comercial Jafra, S.A. de C.V. 9895a320-8a74-4b27-9bf1-4b492f89888c 2025-10-21 Warnings Exact identifier application number: M016 JAFRA Fruteria So Citrico DIMETHICONE Distribuidora Comercial Jafra, S.A. de C.V. a68d6cda-2268-440a-9ca6-677c4e3ea0e7 2025-10-21 Warnings Exact identifier application number: M016 JAFRA Fruteria Very Verde Lip Balm DIMETHICONE Distribuidora Comercial Jafra, S.A. de C.V. 4f0de70b-7ebe-4381-9b46-d5b334f426e0 2025-10-21 Warnings Exact identifier application number: M016 Gelmicin Hydrocortisone with Aloe HYDROCORTISONE United Exchange Corp. bb64eca4-799d-4711-e053-2995a90af403 2025-10-21 Warnings Exact identifier application number: M016 Quadrydern HYDROCORTISONE Productos Zapotol Corp a087ad4d-9a65-19c3-e053-2995a90ab341 2025-10-21 Warnings Exact identifier application number: M016 VENROCK ROSEMARY OIL Guangzhou Oupeng Cosmetics Co., Ltd 4156b669-1817-6280-e063-6394a90aaf3a 2025-10-17 Warnings Exact identifier application number: M016 Gerigentle-Vitamins A and D PETROLATUM Geri-Gentle Corporation c36c74f7-975b-4e4c-99e3-e6921d782c71 2025-10-17 Warnings Exact identifier application number: M016 Seacall Dexamethasone Ointment. DEXAMETHASONE OINTMENT Guangdong Quadrant Ecological Technology Co., Ltd. 201adf67-773c-34a2-e063-6394a90ac525 2025-10-15 Warnings Exact identifier application number: M016 Medline ZINC OXIDE Medline Industries, LP dae45414-7401-9536-e053-2a95a90a0a86 2025-10-15 Warnings Exact identifier application number: M016 Curology Barrier Balm SKIN BARRIER BALM Curology 04b2ba38-0f81-be51-e063-6294a90af821 2025-10-15 Warnings Exact identifier application number: M016 Petroleum WHITE PETROLATUM Medline Industries, LP 34f3581f-39ba-4f28-9237-52f3820ab4c0 2025-10-09 Warnings Exact identifier application number: M016 Facial Fortress PYRITHIONE ZINC Pediatric Solutions, LLC cdd3c52e-4c32-46c1-bdb3-957b164190bb 2025-10-08 Warnings Exact identifier application number: M016 Happy Cappy PYRITHIONE ZINC Pediatric Solutions, LLC 3d3828d8-ee15-4aff-99d1-a121f0102a00 2025-10-08 Warnings Exact identifier application number: M016 Purforma Advanced Hand Sanitizer 70% Alcohol HAND SANITIZER 70% ALCOHOL Spartan Chemical Company, Inc. 06bd825d-914f-5ca7-e063-6394a90aec49 2025-10-06 Warnings Exact identifier application number: M016 Scar Reducer Intensive Herbal and Nutrient ALLANTOIN Quantum, Inc 5197f1fa-aae5-406c-97d9-635b8c1a88a8 2025-10-06 Warnings Exact identifier application number: M016 PURE SOL SPF 30 LIP BALM CACOA BUTTER ZINC OXIDE Brand 2022b LLC 40537561-d334-5859-e063-6394a90a92a7 2025-10-04 Warnings Exact identifier application number: M016 PURE SOL SPF15 Lip Gloss original ZINC OXIDE Brand 2022b LLC 4056e49a-2976-38f9-e063-6394a90a786d 2025-10-04 Warnings Exact identifier application number: M016 PURE SOL SPF15 Lip Gloss Nudie rose ZINC OXIDE Brand 2022b LLC 4057b0e2-1c31-abae-e063-6294a90a053d 2025-10-04 Warnings Exact identifier application number: M016 PURE SOL SPF15 Lip Gloss Pink coral ZINC OXIDE Brand 2022b LLC 405865dd-7d0e-048d-e063-6394a90ab105 2025-10-04 Warnings Exact identifier application number: M016 HealthWise Medicated Diabetic Foot Cream DIMETHICONE, PETROLATUM Veridian Healthcare 164f4cd8-975a-40d5-e063-6394a90ae7d5 2025-10-02 Warnings Exact identifier application number: M016
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 69148-001-00 69148000100 118.6 g in 1 TUBE (69148-001-00) 118.6 g 2014-08-06 0000-00-00 No No Current 69148-001-01 69148000101 60 g in 1 TUBE (69148-001-01) 60 g 2018-01-01 0000-00-00 Yes No Current 69148-001-02 69148000102 100 g in 1 TUBE (69148-001-02) 100 g 2024-04-22 No No Current