Sunscreen SPF30
- Product NDC
- 71513-708
- 11-digit product format
- 715130708
- Labeler code
- 71513
- Product ID
- 71513-708_43d0ff9a-d19e-ab24-e063-6394a90a107c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- avobenzone, homosalate, octisalate, octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Broder Bros Prime Line
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-09
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71513-708-01 | Sunscreen SPF30 | 29.6 mL in 1 BOTTLE | LOTION | 29.6 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71513-708-01 | 71513070801 | 29.6 mL in 1 BOTTLE (71513-708-01) | 29.6 ml | 2025-08-09 | No | No | Historical |