SPF 30 Daily Sunscreen
- Product NDC
- 81136-001
- Requested package NDC
- 81136-001-01
- 11-digit product format
- 811360001
- Labeler code
- 81136
- Product ID
- 81136-001_c0541f32-f073-3630-e053-2a95a90a12d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Brand Evangelists for Beauty Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-04-19
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 220 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81136-001-01 | SPF 30 Daily Sunscreen | 50 mL in 1 TUBE | CREAM | 50 | | 8 |
| 81136-001-01 | SPF 30 Daily Sunscreen | 1 in 1 CARTON | CREAM | 1 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81136-001 | SPF 30 DAILY SUNSCREEN (ZINC OXIDE) CREAM [BRAND EVANGELISTS FOR BEAUTY LTD.] | 8 | Legacy NDC, 2 package rows | 20240228_c0541f32-f072-3630-e053-2a95a90a12d6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81136-001-01 | 81136000101 | 1 TUBE in 1 CARTON (81136-001-01) > 50 mL in 1 TUBE | 1 tube | 2021-04-19 | 0000-00-00 | No | No | Current |