Dr. Nikko Sheer Sunscreen Broad Spectrum SPF 40
- Product NDC
- 71651-001
- 11-digit product format
- 716510001
- Labeler code
- 71651
- Product ID
- 71651-001_996f7989-17d1-5b28-e053-2995a90af8b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OCTISALATE, and ENSULIZOLE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Nikko Cosmetic Surgery Center
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-05-01
- Marketing end
- 2021-06-30
- Substance
- OCTINOXATE; OCTISALATE; ENSULIZOLE
- Active strength
- 70 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 71651-001-01 | 71651000101 | 1 TUBE in 1 CARTON (71651-001-01) > 50 mL in 1 TUBE | 1 tube | 2018-05-01 | 2021-06-30 | No | No | Current |