Petrolatum
- Product NDC
- 72288-180
- 11-digit product format
- 722880180
- Labeler code
- 72288
- Product ID
- 72288-180_5cc92f0c-18ed-af78-e063-6394a90a559d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petrolatum
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Amazon.com Services LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-04-25
- Substance
- PETROLATUM
- Active strength
- 410 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 72288-180 | 72288-180-17 | D | Discontinued by firm | 2026-10-21 |
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.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
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
- Petrolatum
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| PETROLATUM | 410 mg/g |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72288-180-17 | Petrolatum | 50 g in 1 TUBE | OINTMENT | 50 | 21 | |
| 72288-180-41 | Petrolatum | 396 g in 1 JAR | OINTMENT | 396 | 21 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Anubis Barcelona New Even | LACTIC ACID, CITRIC ACID, GLYCOLIC ACID | ANUBIS COSMETICS SL | eaeeb6e0-5322-20c4-e053-2995a90a9fd9 | 2023-09-01 | Warnings | M016 |
| Anubis Barcelona Vital Line | HYDROLYZED COLLAGEN | ANUBIS COSMETICS SL | f564bbf0-3b5c-4a81-e053-2a95a90a7ea6 | 2023-08-29 | Warnings | M016 |
| Carmex Classic Lip Balm Medicated Free Cupcake Batter Stick Sunscreen SPF 15 | CAMPHOR (SYNTHETIC), PETROLATUM | Carma Laboratories, Inc. | 5378d653-702d-405c-a067-882554aaf93a | 2023-08-21 | Warnings | M016 |
| Quality Choice Anti-itch Medicated | CALAMINE AND PRAMOXINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION INC | 5e07f26f-cfb6-57f9-e053-2991aa0a2008 | 2023-08-02 | Warnings | M016 |
| Barrier Balm | BARRIER BALM | Autumn Harp, Inc. | 01df9746-991b-4363-e063-6294a90aaac6 | 2023-08-01 | Warnings | M016 |
| Barrier Cream | ZINC OXIDE | Avasol LLC | bc6a2736-faa6-46d3-af9b-a70f0762e9ce | 2023-05-15 | Warnings | M016 |
| First Aid Beauty FAB Ultra Repair Skin Protectant Candy Cane | COLLOIDAL OATMEAL | The Procter & Gamble Manufacturing Company | bec2f702-5ff5-ea66-e053-2a95a90ad1ec | 2023-01-01 | Warnings | M016 |
| Badger After-BUG Balm | COLLOIDAL OATMEAL | W.S. Badger Company, Inc. | a623da47-cef2-146f-e053-2a95a90afe3a | 2021-11-17 | Warnings | M016 |
| Derma-e Eczema Relief | OATMEAL | Topiderm, Inc | e1797f81-af4b-49e1-9906-dbfd904a282b | 2020-08-19 | Warnings | M016 |
| Resurfix Plus | PETROLATUM | Topiderm, Inc. | f100f43d-6ace-4c3a-9c85-640c0ab2e360 | 2019-11-19 | Warnings | M016 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 725145 | petrolatum 41 % Topical Ointment | PSN | 833b5af7-8db1-4f88-bf4d-9cf32c7cf795 | 21 |
| 725145 | petrolatum 0.41 MG/MG Topical Ointment | SCD | 833b5af7-8db1-4f88-bf4d-9cf32c7cf795 | 21 |
| 725145 | petrolatum 41 % Topical Ointment | SY | 833b5af7-8db1-4f88-bf4d-9cf32c7cf795 | 21 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72288-180-17 | 72288018017 | 50 g in 1 TUBE (72288-180-17) | 50 g | 2018-04-25 | 0000-00-00 | No | No | Current |
| 72288-180-41 | 72288018041 | 396 g in 1 JAR (72288-180-41) | 396 g | 2018-04-25 | 0000-00-00 | No | No | Current |