BIOSOLIS Face Sunscreen broad spectrum SPF30
- Product NDC
- 61296-018
- 11-digit product format
- 612960018
- Labeler code
- 61296
- Product ID
- 61296-018_eff52842-7643-c4ec-e053-2995a90a6dc3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Pro Vera SA
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-01-07
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 188 mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61296-018-00 | 61296001800 | 1 BOTTLE, PUMP in 1 BOX (61296-018-00) > 50 mL in 1 BOTTLE, PUMP | 2022-01-07 | 0000-00-00 | No | No | Current |