ALOE UP
- Product NDC
- 13630-0182
- 11-digit product format
- 136300182
- Labeler code
- 13630
- Product ID
- 13630-0182_cf5a8d49-7929-56fd-e053-2995a90a0e65
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Octisalate, Avobenzone, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Packaging Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-09-28
- Marketing end
- 0000-00-00
- Substance
- OCTOCRYLENE; AVOBENZONE; OCTISALATE; HOMOSALATE
- Active strength
- 28 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 13630-0182-4 | 13630018204 | 156 g in 1 CANISTER (13630-0182-4) | 156 g | 2015-09-28 | 0000-00-00 | No | No | Current |