BIOSOLIS Face Sunscreen Broadspectrum SPF50
- Product NDC
- 61296-017
- 11-digit product format
- 612960017
- Labeler code
- 61296
- Product ID
- 61296-017_eff50342-b869-24d4-e053-2a95a90a851f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, 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
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 100 mg/mL; 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 |
|---|
| 61296-017-00 | 61296001700 | 1 BOTTLE, PUMP in 1 BOX (61296-017-00) > 50 mL in 1 BOTTLE, PUMP | 2022-01-07 | 0000-00-00 | No | No | Current |