ALOE UP
- Product NDC
- 13630-0206
- 11-digit product format
- 136300206
- Labeler code
- 13630
- Product ID
- 13630-0206_d5ddc9a0-2d22-22e6-e053-2995a90a00d5
- 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
- 2016-11-10
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 25 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13630-0206-4 | 13630020604 | 186 mL in 1 CANISTER (13630-0206-4) | 186 ml | 2016-11-10 | 0000-00-00 | No | No | Current |