Srubs Sunscreen
- Product NDC
- 51239-4921
- 11-digit product format
- 512394921
- Labeler code
- 51239
- Product ID
- 51239-4921_4538b23e-3bd5-cefb-e063-6294a90a58f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- ITW Pro Brands
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-02
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 7; 5; 5 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Srubs Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 3 g/100g |
| HOMOSALATE | 7 g/100g |
| OCTISALATE | 5 g/100g |
| OCTOCRYLENE | 5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51239-4921-1 | Srubs Sunscreen | 7 g in 1 PACKET | LOTION | 7 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51239-4921 | SRUBS SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [ITW PRO BRANDS] | 3 | Current NDC, 1 package rows | 20241016_06c1dc42-5a01-f898-e063-6394a90a1a1a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51239-4921-1 | 51239492101 | 7 g in 1 PACKET (51239-4921-1) | 7 g | 2023-10-02 | No | No | Historical |