Hampton Sun SPF 50
- Product NDC
- 72667-031
- Requested package NDC
- 72667-031-01
- 11-digit product format
- 726670031
- Labeler code
- 72667
- Product ID
- 72667-031_e24a8ab9-758e-5e5d-e053-2a95a90a1d41
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Humosalate, Octisalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Inspec Solutions
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-06-25
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72667-031-01 | 72667003101 | 150 mL in 1 CAN (72667-031-01) | 150 ml | 2022-06-25 | 0000-00-00 | No | No | Current |