Home NDC 41250-059 Healing
Product NDC 41250-059
11-digit product format 412500059
Labeler code 41250
Product ID 41250-059_4b32672c-1f60-aade-e063-6394a90ad912
Type HUMAN OTC DRUG
Nonproprietary name Petrolatum
Dosage form OINTMENT
Route TOPICAL
Labeler Meijer, Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-08-01
Substance PETROLATUM
Active strength 410 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 41250-059 41250-059-16 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 41250-059 41250-059-16 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 Healing
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM 410 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4T6H12BN9U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 725145 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-059-16 Healing 56 g in 1 TUBE OINTMENT 56 16 41250-059-17 Healing 50 g in 1 TUBE OINTMENT 50 16 41250-059-41 Healing 396 g in 1 JAR OINTMENT 396 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Petrolatum ACTIVE INGREDIENT 4T6H12BN9U HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 PETROLATUM ACTIVE MOIETY 4T6H12BN9U HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 CERESIN INACTIVE INGREDIENT Q1LS2UJO3A HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 LANOLIN ALCOHOLS INACTIVE INGREDIENT 884C3FA9HE HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 LEVOMENOL INACTIVE INGREDIENT 24WE03BX2T HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2 PANTHENOL INACTIVE INGREDIENT WV9CM0O67Z HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-059 HEALING (PETROLATUM) OINTMENT [MEIJER DISTRIBUTION, INC] 15 Current NDC, Legacy NDC, 3 package rows 20250515_8cb56ee4-b9d1-4a29-88c7-e6f3ac2112c1.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 66 of 70 · 1,384 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Calm and Heal Melting Balm ALLANTOIN The Honest Company, Inc. b08a1bd6-986d-9520-e053-2995a90a865e 2023-12-19 Warnings Exact identifier application number: M016 TopCare Calagesic CALAMINE AND PRAMOXINE HYDROCHLORIDE LOTION TOPCO ASSOCIATES LLC 8dced3ea-147b-3d46-e053-2a95a90aa1c0 2023-12-18 Warnings Exact identifier application number: M016 TopCare Calamine CALAMINE 8% AND ZINC OXIDE 8% LOTION TOPCO ASSOCIATES LLC 8dcf134e-0427-0c43-e053-2995a90a7c26 2023-12-18 Warnings Exact identifier application number: M016 HEB Calaclear ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE H E B 5d576794-88d1-484a-e053-2991aa0aa479 2023-12-18 Warnings Exact identifier application number: M016 Publix Calamine Medicated ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE Publix 5d6ba4cf-f2cb-0ecb-e053-2991aa0a5673 2023-12-18 Warnings Exact identifier application number: M016 TopCare Calaclear PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE LOTION TOPCO ASSOCIATES LLC 8dce8817-b905-4064-e053-2995a90a071e 2023-12-18 Warnings Exact identifier application number: M016 Assured Calamine CALAMINE 8% AND ZINC OXIDE 8% Greenbriar International 9d378cc5-9af0-1389-e053-2995a90a0b96 2023-12-18 Warnings Exact identifier application number: M016 HEB Calagesic ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE H E B 5d579680-6bcb-1161-e053-2991aa0aead1 2023-12-18 Warnings Exact identifier application number: M016 Publix Clear Anti-Itch ZINC ACETATE AND PRAMOXINE HYDROCHLORIDE Publix 5d6b905f-ed30-1ab7-e053-2a91aa0a816b 2023-12-18 Warnings Exact identifier application number: M016 Humco Calaclear PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE Humco Holding Group, Inc. 5fca3a73-6d66-496b-bd33-6e044f9039bc 2023-12-15 Warnings Exact identifier application number: M016 Calamine Phenolated Topical Suspension CALAMINE AND ZINC OXIDE AND PHENOL Humco Holding Group, Inc a3816729-be2b-4b4f-a609-953576cd2e3b 2023-12-15 Warnings Exact identifier application number: M016 Humco Mineral Oil Light MINERAL OIL Humco Holding Group, Inc. 753f35c3-1420-4817-ba63-b737a9c99a1d 2023-12-15 Warnings Exact identifier application number: M016 Humco Witch Hazel WITCH HAZEL Humco Holding Group, Inc. 3cf07016-a129-49ca-8fad-b67dda5aa009 2023-12-15 Warnings Exact identifier application number: M016 Rite Aid Calamine CALAMINE 8% AND ZINC OXIDE 8% Rite Aid Corporation 5df71189-9b36-9dee-e053-2a91aa0a9e49 2023-12-15 Warnings Exact identifier application number: M016 GNP Witch Hazel WITCH HAZEL Amerisource Bergen 45ac839d-215d-4c5f-8ae5-5e111d170061 2023-12-14 Warnings Exact identifier application number: M016 La Roche Posay Laboratoire Dermatologique Cicaplast Defense B5 Skin Protectant GLYCERIN L'Oreal USA Products Inc 32eaaaab-41bd-4efe-a71d-92e3a702c1e5 2023-12-11 Warnings Exact identifier application number: M016 La Roche Posay Laboratoire Dermatologique Lipikar Eczema Relief OATMEAL COSMETIQUE ACTIVE PRODUCTION e555de17-9b42-4125-a17b-467bc1d179d7 2023-12-11 Warnings Exact identifier application number: M016 La Roche Posay Laboratoire Dermatologique Lipikar Eczema Soothing Relief OATMEAL L'Oreal USA Products Inc f7b71606-0044-4729-82e8-4514331806a0 2023-12-11 Warnings Exact identifier application number: M016 La Roche Posay Laboratoire Dermatologique Cicaplast Defense B5 GLYCERIN Cosmetique Active Production 01c8a0d5-bcd1-4639-be45-530a226401f0 2023-12-11 Warnings Exact identifier application number: M016 Carmex Classic Lip Balm Medicated Free Cupcake Batter Stick Sunscreen SPF 15 CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONE Carma Laboratories, Inc. 0bc6812a-5c2a-7bb9-e063-6294a90a36e3 2023-12-05 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 41250-059-16 41250005916 56 g in 1 TUBE (41250-059-16) 56 g 2013-08-01 0000-00-00 No No Current 41250-059-17 41250005917 50 g in 1 TUBE (41250-059-17) 50 g 2013-08-01 0000-00-00 No No Current 41250-059-41 41250005941 396 g in 1 JAR (41250-059-41) 396 g 2023-11-03 No No Current