warnings
Warnings For external use only
Aquaphor Lip Protectant and Sunscreen
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 Lip Protectant and Sunscreen
- Generic name
- PETROLATUM, AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
- Manufacturer
- Beiersdorf Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a43c2802-9cf1-477e-9f93-e11cf40b480d
- SPL ID
- 46043588-4988-0a04-e063-6394a90a5145
- Version
- 10
- Effective date
- 2025-12-15
- Source export date
- 2026-10-30
- 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/2026-10-30/57469fe40e5b1c0d9604dc7dbc22532ea48e8e53acfb911fc676578d98492f7e/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:30:28
| 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 Lip Protectant and Sunscreen | openfda.brand_name | |
| generic name | PETROLATUM, AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE | openfda.generic_name | |
| manufacturer name | Beiersdorf Inc | openfda.manufacturer_name | |
| ndc | package | 10356-111-40 | openfda.package_ndc |
| ndc | package | 10356-111-30 | openfda.package_ndc |
| ndc | package | 10356-111-23 | openfda.package_ndc |
| ndc | product | 10356-111 | openfda.product_ndc |
| ndc11 | package | 10356011130 | derived:openfda.package_ndc |
| ndc11 | package | 10356011140 | derived:openfda.package_ndc |
| ndc11 | package | 10356011123 | derived:openfda.package_ndc |
| spl id | 46043588-4988-0a04-e063-6394a90a5145 | id | |
| spl set id | a43c2802-9cf1-477e-9f93-e11cf40b480d | set_id | |
| unii | 95OOS7VE0Y | openfda.unii | |
| unii | 4T6H12BN9U | openfda.unii | |
| unii | 5A68WGF6WM | openfda.unii | |
| unii | G63QQF2NOX | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii | |
| unii | 4Y5P7MUD51 | 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.