SUNSCREEN
- Product NDC
- 79481-0025
- Requested package NDC
- 79481-0025-3
- 11-digit product format
- 794810025
- Labeler code
- 79481
- Product ID
- 79481-0025_de6c1d3b-8381-4da3-ac62-3c3aad4293a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalat, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Meijer
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-11-30
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 90 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79481-0025 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALAT, OCTOCRYLENE) LOTION [MEIJER DISTRIBUTION, INC] | 3 | Legacy NDC | 20240824_0d3687f5-473f-4d4d-af5e-24832ff520e6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79481-0025-3 | 79481002503 | 88 mL in 1 TUBE (79481-0025-3) | 88 ml | 2021-11-30 | 0000-00-00 | No | No | Current |