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- Product NDC
- 49404-134
- 11-digit product format
- 494040134
- Labeler code
- 49404
- Product ID
- 49404-134_30bb91c5-56bc-40c7-8d4f-8b27af87ead0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Have & Be Co., Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-10-21
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE
- Active strength
- 2 mg/30mL; mg/30mL; mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record