SUN ULTIMATE FACE SPF 30
- Product NDC
- 14324-020
- 11-digit product format
- 143240020
- Labeler code
- 14324
- Product ID
- 14324-020_d4db1b95-5105-dd3a-e053-2a95a90a88f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTISALATE, AVOBENZONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Naos USA, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTISALATE; AVOBENZONE
- Active strength
- 90 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 14324-020-50 | 14324002050 | 1 TUBE in 1 BOX (14324-020-50) > 50 mL in 1 TUBE | 1 tube | 2019-04-01 | 0000-00-00 | No | No | Current |