warnings
When using this product • do not get into eyes
Aquaphor Healing
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 Healing
- Generic name
- PETROLATUM
- Manufacturer
- Beiersdorf Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0a17bf6f-6114-4647-a509-65999255c37b
- SPL ID
- 460350b1-7ff7-de4e-e063-6294a90aaae4
- Version
- 20
- Effective date
- 2025-12-15
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:58
| 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 Healing | openfda.brand_name | |
| generic name | PETROLATUM | openfda.generic_name | |
| manufacturer name | Beiersdorf Inc | openfda.manufacturer_name | |
| ndc | package | 10356-101-39 | openfda.package_ndc |
| ndc | package | 10356-101-40 | openfda.package_ndc |
| ndc | package | 10356-101-43 | openfda.package_ndc |
| ndc | package | 10356-101-57 | openfda.package_ndc |
| ndc | package | 10356-101-50 | openfda.package_ndc |
| ndc | package | 10356-101-30 | openfda.package_ndc |
| ndc | package | 10356-101-10 | openfda.package_ndc |
| ndc | package | 10356-101-37 | openfda.package_ndc |
| ndc | package | 10356-101-29 | openfda.package_ndc |
| ndc | package | 10356-101-42 | openfda.package_ndc |
| ndc | package | 10356-101-49 | openfda.package_ndc |
| ndc | package | 10356-101-44 | openfda.package_ndc |
| ndc | package | 10356-101-06 | openfda.package_ndc |
| ndc | package | 10356-101-02 | openfda.package_ndc |
| ndc | package | 10356-101-38 | openfda.package_ndc |
| ndc | package | 10356-101-08 | openfda.package_ndc |
| ndc | package | 10356-101-23 | openfda.package_ndc |
| ndc | package | 10356-101-04 | openfda.package_ndc |
| ndc | package | 10356-101-35 | openfda.package_ndc |
| ndc | product | 10356-101 | openfda.product_ndc |
| ndc11 | package | 10356010137 | derived:openfda.package_ndc |
| ndc11 | package | 10356010157 | derived:openfda.package_ndc |
| ndc11 | package | 10356010149 | derived:openfda.package_ndc |
| ndc11 | package | 10356010123 | derived:openfda.package_ndc |
| ndc11 | package | 10356010140 | derived:openfda.package_ndc |
| ndc11 | package | 10356010138 | derived:openfda.package_ndc |
| ndc11 | package | 10356010142 | derived:openfda.package_ndc |
| ndc11 | package | 10356010139 | derived:openfda.package_ndc |
| ndc11 | package | 10356010150 | derived:openfda.package_ndc |
| ndc11 | package | 10356010135 | derived:openfda.package_ndc |
| ndc11 | package | 10356010130 | derived:openfda.package_ndc |
| ndc11 | package | 10356010102 | derived:openfda.package_ndc |
| ndc11 | package | 10356010143 | derived:openfda.package_ndc |
| ndc11 | package | 10356010110 | derived:openfda.package_ndc |
| ndc11 | package | 10356010106 | derived:openfda.package_ndc |
| ndc11 | package | 10356010104 | derived:openfda.package_ndc |
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.