Panama Jack
- Product NDC
- 13630-0030
- 11-digit product format
- 136300030
- Labeler code
- 13630
- Product ID
- 13630-0030_9c5c735f-5834-37d1-e053-2995a90ae48c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ocinoxate, Octisalate, and Oxybenzone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Packaging, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-12-30
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 41 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 |
|---|
| 13630-0030-4 | 13630003004 | 177 mL in 1 CAN (13630-0030-4) | 177 ml | 2011-12-30 | 0000-00-00 | No | No | Current |