BABY SUNSCREEN
- Product NDC
- 42263-101
- 11-digit product format
- 422630101
- Labeler code
- 42263
- Product ID
- 42263-101_ff916fda-5163-48a5-92df-f4a049cc94a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- SEVENTH GENERATION INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-12-30
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 20 g/100g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42263-101-13 | BABY SUNSCREENSPF 30 | 85 g in 1 TUBE | LOTION | 85 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42263-101 | BABY SUNSCREEN SPF 30 (ZINC OXIDE) LOTION [SEVENTH GENERATION INC] | 4 | Legacy NDC, 1 package rows | 20120327_c17dec08-5749-424d-8139-1fc0a10515de.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42263-101-13 | 42263010113 | 85 g in 1 TUBE | 85 g | Historical |