Baby blanket
- Product NDC
- 58443-0092
- 11-digit product format
- 584430092
- Labeler code
- 58443
- Product ID
- 58443-0092_9c5941d2-59e5-a016-e053-2a95a90a4fea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide, and Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Prime Enterprises, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-12-23
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 77 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58443-0092-4 | 58443009204 | 180 mL in 1 BOTTLE (58443-0092-4) | 180 ml | 2013-12-23 | 0000-00-00 | No | No | Current |