Private Label Sunscreen SPF35 40min WR RE126-202
- Product NDC
- 60232-0036
- 11-digit product format
- 602320036
- Labeler code
- 60232
- Product ID
- 60232-0036_fe000ceb-250f-465c-81cf-ed3d78f0e7f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- homosalate, zinc oxide sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Swiss-American CDMO, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-09
- Substance
- HOMOSALATE; OCTISALATE; ZINC OXIDE
- Active strength
- 90; 50; 100 g/1000g; g/1000g; g/1000g
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60232-0036-1 | Private Label Sunscreen SPF35 40min WR RE126-202 | 30 g in 1 PACKAGE | LOTION | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60232-0036 | PRIVATE LABEL SUNSCREEN SPF35 40MIN WR RE126-202 (HOMOSALATE, ZINC OXIDE SUNSCREEN) LOTION [SWISS-AMERICAN CDMO, LLC] | 1 | Current NDC, 1 package rows | 20231110_254fa69f-2413-47e8-bc9b-5b7b0b59a5c8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60232-0036-1 | 60232003601 | 30 g in 1 PACKAGE (60232-0036-1) | 30 g | 2023-11-09 | No | No | Historical |