LifeCell
- Product NDC
- 58443-0439
- 11-digit product format
- 584430439
- Labeler code
- 58443
- Product ID
- 58443-0439_cf6fdc1f-7fb4-2f88-e053-2a95a90aac15
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Prime Enterprises Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-10-23
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 31 mg/mL; mg/mL
- 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 |
|---|---|---|---|---|---|---|---|---|
| 58443-0439-3 | 58443043903 | 50 mL in 1 BOTTLE (58443-0439-3) | 50 ml | 2015-10-23 | 0000-00-00 | No | No | Current |