Sunscreen
- Product NDC
- 0869-0790
- 11-digit product format
- 008690790
- Labeler code
- 0869
- Product ID
- 0869-0790_293e211c-cb28-4791-bace-53817f58c44d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-08-07
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 26 mg/g; mg/g; mg/g; mg/g; mg/g
- 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 |
|---|
| 0869-0790-30 | 00869079030 | 170 g in 1 BOTTLE, SPRAY (0869-0790-30) | 170 g | 2017-08-07 | 0000-00-00 | No | No | Current |