Neova DNA Damage Control - Everyday
- Product NDC
- 72251-002
- Requested package NDC
- 72251-002-74
- 11-digit product format
- 722510002
- Labeler code
- 72251
- Product ID
- 72251-002_ee524e0f-f649-1d75-e053-2a95a90adde7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Zinc Oxide
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- PHARMA COSMETICS, INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-10-08
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; ZINC OXIDE
- Active strength
- 7 g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 72251-002-74 | 72251000274 | 74 mL in 1 BOTTLE (72251-002-74) | 74 ml | 2018-04-19 | 0000-00-00 | No | No | Current |