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- Product NDC
- 13630-0116
- 11-digit product format
- 136300116
- Labeler code
- 13630
- Product ID
- 13630-0116_e1f6b563-1182-90fe-e053-2a95a90a0237
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Packaging Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-08-17
- Marketing end
- 2023-08-31
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE
- Active strength
- 25 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 13630-0116-4 | 13630011604 | 177 mL in 1 CAN (13630-0116-4) | 177 ml | 2016-08-17 | 0000-00-00 | No | No | Current |