Sunscreen
- Product NDC
- 72476-926
- Requested package NDC
- 72476-926-14
- 11-digit product format
- 724760926
- Labeler code
- 72476
- Product ID
- 72476-926_03d98704-58e8-4234-9a04-9e57d70337f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Retail Business Services, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-10-28
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72476-926-14 | Sunscreen | 156 g in 1 BOTTLE, SPRAY | SPRAY | 156 | | 7 |
| 72476-926-15 | Sunscreen | 258 g in 1 BOTTLE, SPRAY | SPRAY | 258 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72476-926 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [RETAIL BUSINESS SERVICES, LLC] | 5 | Legacy NDC, 2 package rows | 20240907_2467dd9b-44ae-4354-9b75-4606204ff042.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72476-926-14 | 72476092614 | 156 g in 1 BOTTLE, SPRAY (72476-926-14) | 156 g | 2020-10-28 | 0000-00-00 | No | No | Current |