Stout Daily SPF for Men
- Product NDC
- 71100-001
- 11-digit product format
- 711000001
- Labeler code
- 71100
- Product ID
- 71100-001_b4e2c44e-3027-45d1-969c-bd3e6596fcd5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Stout Face Care Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-03-01
- Substance
- ZINC OXIDE
- Active strength
- 8.82 g/90mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stout Daily SPF for Men
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 8.82 g/90mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71100-001-90 | Stout Daily SPF for Men | 90 mL in 1 TUBE | LIQUID | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71100-001 | STOUT DAILY SPF FOR MEN (SUNSCREEN) LIQUID [STOUT FACE CARE INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20170301_cebbb3b5-4a68-4fbb-a12e-4e46a04c82dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71100-001-90 | 71100000190 | 90 mL in 1 TUBE (71100-001-90) | 90 ml | 2017-03-01 | 0000-00-00 | No | No | Current |