ALOE UP
- Product NDC
- 58443-0300
- 11-digit product format
- 584430300
- Labeler code
- 58443
- Product ID
- 58443-0300_a4d6cfa9-2a4f-2398-e053-2995a90a662c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octisalate, Avobenzone, Homosalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Enterprises Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE; OCTINOXATE
- Active strength
- 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58443-0300-3 | 58443030003 | 89 mL in 1 BOTTLE (58443-0300-3) | 89 ml | 2018-07-09 | 0000-00-00 | No | No | Current |