Avobenzone, Homosalate, Octisalate, Octocrylene
- Product NDC
- 0869-0714
- 11-digit product format
- 008690714
- Labeler code
- 0869
- Product ID
- 0869-0714_6c5ddf32-e5e3-478b-a6ee-1434f61d2c45
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-11-28
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30 mg/mL; 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 |
|---|
| 0869-0714-18 | 00869071418 | 74 mL in 1 BOTTLE, PLASTIC (0869-0714-18) | 74 ml | 2016-11-28 | 0000-00-00 | No | No | Current |
| 0869-0714-34 | 00869071434 | 236 mL in 1 BOTTLE, PLASTIC (0869-0714-34) | 236 ml | 2016-11-28 | 0000-00-00 | No | No | Current |
| 0869-0714-38 | 00869071438 | 296 mL in 1 BOTTLE, PLASTIC (0869-0714-38) | 296 ml | 2016-11-28 | 0000-00-00 | No | No | Current |