Proactiv SPF 15
- Product NDC
- 11410-026
- 11-digit product format
- 114100026
- Labeler code
- 11410
- Product ID
- 11410-026_9a445b5a-87c0-4132-9c85-9192257be08a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, and Octocrylene
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- THE PROACTIV COMPANY LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-07-20
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 6 mg/100mL; mg/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 11410-026-00 | 11410002600 | 1 TUBE in 1 BOX (11410-026-00) > 20 mL in 1 TUBE | 1 tube | 2015-07-20 | 0000-00-00 | No | No | Current |