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
- Jell Pharmaceuticals Pvt. Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- cd848f33-e863-d3af-e053-2a95a90a45b1
- SPL ID
- 29768db2-7b93-f182-e063-6394a90a0ad3
- Version
- 2
- Effective date
- 2024-12-17
- Source export date
- 2026-10-12
- 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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:44:12
| 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 | Jell Pharmaceuticals Pvt. Ltd. | openfda.manufacturer_name | |
| ndc | package | 30400-501-07 | openfda.package_ndc |
| ndc | package | 30400-501-06 | openfda.package_ndc |
| ndc | package | 30400-501-08 | openfda.package_ndc |
| ndc | package | 30400-501-01 | openfda.package_ndc |
| ndc | package | 30400-501-04 | openfda.package_ndc |
| ndc | package | 30400-501-03 | openfda.package_ndc |
| ndc | package | 30400-501-05 | openfda.package_ndc |
| ndc | package | 30400-501-02 | openfda.package_ndc |
| ndc | product | 30400-501 | openfda.product_ndc |
| ndc11 | package | 30400050105 | derived:openfda.package_ndc |
| ndc11 | package | 30400050103 | derived:openfda.package_ndc |
| ndc11 | package | 30400050107 | derived:openfda.package_ndc |
| ndc11 | package | 30400050108 | derived:openfda.package_ndc |
| ndc11 | package | 30400050104 | derived:openfda.package_ndc |
| ndc11 | package | 30400050101 | derived:openfda.package_ndc |
| ndc11 | package | 30400050106 | derived:openfda.package_ndc |
| ndc11 | package | 30400050102 | derived:openfda.package_ndc |
| rxcui | 1252009 | openfda.rxcui | |
| spl id | 29768db2-7b93-f182-e063-6394a90a0ad3 | id | |
| spl set id | cd848f33-e863-d3af-e053-2a95a90a45b1 | 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.