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- Product NDC
- 68577-040
- 11-digit product format
- 685770040
- Labeler code
- 68577
- Product ID
- 68577-040_2a2fa1cb-5ea6-dc69-e063-6394a90a0087
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Cosmax Usa, Corporation
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 20; 90; 45; 20 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| G63QQF2NOX | AVOBENZONE | 70356-09-1 | AVOBENZONE |
| V06SV4M95S | HOMOSALATE | 118-56-9 | HOMOSALATE |
| 4X49Y0596W | OCTISALATE | 118-60-5 | OCTISALATE |
| 5A68WGF6WM | OCTOCRYLENE | 6197-30-4 | OCTOCRYLENE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68577-040-00 | 68577004000 | 60 mL in 1 BOTTLE (68577-040-00) | 60 ml | 2022-06-01 | No | No | Historical |