warnings
Warnings For external use only When using this product • do not get into eyes
Aquaphor Original
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
- Aquaphor Original
- Generic name
- PETROLATUM
- Manufacturer
- Beiersdorf Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d38ec874-7b8c-4b9b-92b6-286278bb67f3
- SPL ID
- 46041c57-79d9-e56c-e063-6394a90a8783
- Version
- 16
- Effective date
- 2025-12-15
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:50
| 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 | Aquaphor Original | openfda.brand_name | |
| generic name | PETROLATUM | openfda.generic_name | |
| manufacturer name | Beiersdorf Inc | openfda.manufacturer_name | |
| ndc | package | 10356-100-37 | openfda.package_ndc |
| ndc | product | 10356-100 | openfda.product_ndc |
| ndc11 | package | 10356010037 | derived:openfda.package_ndc |
| rxcui | 725145 | openfda.rxcui | |
| rxcui | 1052954 | openfda.rxcui | |
| spl id | 46041c57-79d9-e56c-e063-6394a90a8783 | id | |
| spl set id | d38ec874-7b8c-4b9b-92b6-286278bb67f3 | 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.