BB Care Ultra Light Sunscreen Broad Spectrum SPF 50 Plus
- Product NDC
- 71388-001
- 11-digit product format
- 713880001
- Labeler code
- 71388
- Product ID
- 71388-001_7e0447f6-de04-5089-e053-2a91aa0a8b56
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Beauty Be Co., Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-04-14
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 78 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71388-001-00 | 71388000100 | 1 TUBE in 1 BOX (71388-001-00) > 30 g in 1 TUBE | 1 tube | 2017-04-14 | 0000-00-00 | No | No | Current |