Personalized Day Moisturizer with SPF 50
- Product NDC
- 73572-005
- 11-digit product format
- 735720005
- Labeler code
- 73572
- Product ID
- 73572-005_d06d55a4-455e-1a60-e053-2a95a90ae887
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTISALATE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Proven Skincare
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-11-15
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTISALATE; ZINC OXIDE
- Active strength
- 100 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 |
|---|
| 73572-005-30 | 73572000530 | 30 mL in 1 BOTTLE (73572-005-30) | 30 ml | 2021-11-15 | 0000-00-00 | No | No | Current |