warnings
Warnings For external use only
Shea Butter Petroleum Jelly
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Shea Butter Petroleum Jelly
- Generic name
- PETROLATUM JELLY
- Manufacturer
- Walgreens
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e35d913e-2195-4e3d-ae38-f010317140fd
- SPL ID
- 2973ab35-0fc4-2a64-e063-6294a90aab69
- Version
- 4
- Effective date
- 2024-12-17
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:33:07
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M016 | openfda.application_number | |
| brand name | Shea Butter Petroleum Jelly | openfda.brand_name | |
| generic name | PETROLATUM JELLY | openfda.generic_name | |
| manufacturer name | Walgreens | openfda.manufacturer_name | |
| ndc | package | 0363-0740-13 | openfda.package_ndc |
| ndc | product | 0363-0740 | openfda.product_ndc |
| ndc11 | package | 00363074013 | derived:openfda.package_ndc |
| rxcui | 1252009 | openfda.rxcui | |
| spl id | 2973ab35-0fc4-2a64-e063-6294a90aab69 | id | |
| spl set id | e35d913e-2195-4e3d-ae38-f010317140fd | set_id | |
| unii | 4T6H12BN9U | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.