HEB SPF 50 For Men Sunscreen
- Product NDC
- 37808-044
- 11-digit product format
- 378080044
- Labeler code
- 37808
- Product ID
- 37808-044_24893699-7dc6-dcd2-e063-6394a90a0fa9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE,OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- H.E.B
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-22
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 45; 80 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 |
|---|
| 37808-044-12 | 37808004412 | 237 mL in 1 TUBE (37808-044-12) | 237 ml | 2021-03-22 | No | No | Historical |