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 26 of 68 · 1,357 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join DERMATITIS FACE BALM COLLOIDAL OATMEAL Skinfix, Inc. 86d2db7d-f1d4-4bca-aba4-d4c96b83c1a6 2026-01-08 Warnings Exact identifier application number: M016 First Aid Beauty Dry Skin Rescue Kit 5x Hydration Power COLLOIDAL OATMEAL JCS Global Distribution, Inc. 47d06283-21cd-4a69-e063-6294a90adb05 2026-01-07 Warnings Exact identifier application number: M016 DE LA CRUZ DIAPER RASH ALLANTOIN, PETROLATUM, AND ZINC OXIDE DLC Laboratories, Inc. 5949aa0f-a7cb-453c-81fd-9fa24653a452 2026-01-07 Warnings Exact identifier application number: M016 Thera Wise Natural Hemorrhoidal WITCH HAZEL Derma Wise Skin Care Ltd. a29fb680-cfc8-4a7b-9970-563fa0e2bed6 2026-01-06 Warnings Exact identifier application number: M016 Sky and Sol SPF25 Lip Balm SKY AND SOL SPF25 LIP BALM Guangzhou Fantesy Biotechnology Co.,Ltd 1f37c0c3-6443-60a3-e063-6394a90a596f 2026-01-05 Warnings Exact identifier application number: M016 Remedy Essentials WHITE PETROLATUM,ZINC OXIDE Medline Industries, LP 42a033d6-782b-2d7f-e054-00144ff8d46c 2026-01-05 Warnings Exact identifier application number: M016 BUNUSS Estriol Face ESTRIOL Jiashen International Trade Limited 478b5690-038a-ba1c-e063-6394a90a3ad6 2026-01-04 Warnings Exact identifier application number: M016 Skin Protectant for Babies and kids SKIN PROTECTANT OINTMENT Neilmed Pharmaceuticals Inc. 448b70db-ca81-db7b-e063-6294a90a5f0d 2026-01-02 Warnings Exact identifier application number: M016 Puriya Eczema Cream COLLOIDAL OATMEAL IPC Republic, Inc. 24ac044e-13fa-5ff6-e063-6294a90a9985 2026-01-01 Warnings Exact identifier application number: M016 Scarzen DIMETHICONE Village Pharma LLC 1550f4e5-22e2-491f-8184-de65da7234e6 2026-01-01 Warnings Exact identifier application number: M016 NUVALU 100 PURE PETROLEUM WHITE PETROLATUM JC SALES 48f74b99-7ead-b0d0-e063-6394a90a4929 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM BABY FRESH SCENT WHITE PETROLATUM JC SALES 48f79c2a-b314-169f-e063-6294a90a576e 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM BABY FRESH SCENT WHITE PETROLATUM JC SALES 490ac0a6-eac0-a74f-e063-6394a90a84ed 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM COCOA BUTTER WHITE PETROLATUM JC SALES 490af001-c78c-e2d2-e063-6394a90abdb0 2026-01-01 Warnings Exact identifier application number: M016 NUVALU 100 PURE PETROLEUM WHITE PETROLATUM Ningbo Liyuan Daily Chemical Products Co., Ltd. 4946ac1a-f475-fbb1-e063-6394a90a30bc 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM BABY FRESH SCENT WHITE PETROLATUM Ningbo Liyuan Daily Chemical Products Co., Ltd. 4946d1b7-ae1b-1e73-e063-6394a90a1ed2 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM BABY FRESH SCENT WHITE PETROLATUM Ningbo Liyuan Daily Chemical Products Co., Ltd. 49471d77-303a-8536-e063-6394a90aea51 2026-01-01 Warnings Exact identifier application number: M016 NUVALU PETROLEUM COCOA BUTTER WHITE PETROLATUM Ningbo Liyuan Daily Chemical Products Co., Ltd. 49472319-09d1-7c4f-e063-6294a90a26a7 2026-01-01 Warnings Exact identifier application number: M016 Olay Ultimate Sensitive Colloidal Oatmeal Skin Protectant Moisturizer Fragrance Free COLLOIDAL OATMEAL The Procter & Gamble Manufacturing Company 1fa6282a-172e-f5c8-e063-6294a90a4fb1 2025-12-31 Warnings Exact identifier application number: M016 First Aid Beauty FAB Ultra Repair Skin Protectant Vanilla Latte COLLOIDAL OATMEAL The Procter & Gamble Manufacturing Company 27713ae6-b428-e0d7-e063-6394a90a7a89 2025-12-31 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