Panama Jack
- Product NDC
- 58443-0046
- 11-digit product format
- 584430046
- Labeler code
- 58443
- Product ID
- 58443-0046_9c5a15eb-7863-6750-e053-2a95a90a57ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, and Oxybenzone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Enterprises, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-04-15
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 50 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 |
|---|
| 58443-0046-4 | 58443004604 | 237 mL in 1 BOTTLE (58443-0046-4) | 237 ml | 2013-04-15 | 0000-00-00 | No | No | Current |