ALOE UP
- Product NDC
- 58443-0419
- 11-digit product format
- 584430419
- Labeler code
- 58443
- Product ID
- 58443-0419_cba4648d-c830-6b21-e053-2995a90a9704
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octisalate, Avobenzone, Homosalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Prime Enterprises Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-03-10
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
- Active strength
- 101 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 58443-0419-4 | 58443041904 | 177 mL in 1 BOTTLE (58443-0419-4) | 177 ml | 2020-03-10 | 0000-00-00 | No | No | Current |