SUNZEN
- Product NDC
- 58443-0119
- 11-digit product format
- 584430119
- Labeler code
- 58443
- Product ID
- 58443-0119_9c5a9ebc-5d33-7b1a-e053-2a95a90aad13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Prime Enterprises, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-02-28
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 30 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 |
|---|
| 58443-0119-4 | 58443011904 | 177 mL in 1 TUBE (58443-0119-4) | 177 ml | 2013-02-28 | 0000-00-00 | No | No | Current |