Hampton Sun SPF 30
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
- Hampton Sun SPF 30
- Generic name
- AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 %
- Manufacturer
- S&C Hampton Sun LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- eae99a09-9d9e-459d-af96-aef95a854f94
- SPL ID
- 52538d4d-0843-3bce-e063-6394a90af751
- Version
- 2
- Effective date
- 2026-05-21
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:32
| 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 | M020 | openfda.application_number | |
| brand name | Hampton Sun SPF 30 | openfda.brand_name | |
| generic name | AVOBENZONE 3.00 % OCTISALATE 5.00 % HOMOSALATE 10.00 % | openfda.generic_name | |
| manufacturer name | S&C Hampton Sun LLC | openfda.manufacturer_name | |
| ndc | package | 87170-023-05 | openfda.package_ndc |
| ndc | package | 87170-023-01 | openfda.package_ndc |
| ndc | product | 87170-023 | openfda.product_ndc |
| ndc11 | package | 87170002301 | derived:openfda.package_ndc |
| ndc11 | package | 87170002305 | derived:openfda.package_ndc |
| spl id | 52538d4d-0843-3bce-e063-6394a90af751 | id | |
| spl set id | eae99a09-9d9e-459d-af96-aef95a854f94 | set_id | |
| unii | V06SV4M95S | openfda.unii | |
| unii | G63QQF2NOX | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.