COSRX
- Product NDC
- 70319-220
- 11-digit product format
- 703190220
- Labeler code
- 70319
- Product ID
- 70319-220_4415daaf-9353-7695-e063-6394a90ad88c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Vitamin E Vitalizing Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- COSRX inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 1.25; 4.5; 4.5; 2.25 mg/50mL; mg/50mL; mg/50mL; mg/50mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- COSRX
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 1.25 mg/50mL |
| HOMOSALATE | 4.5 mg/50mL |
| OCTISALATE | 4.5 mg/50mL |
| OCTOCRYLENE | 2.25 mg/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
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 |
|---|
| 70319-220-01 | COSRX | 1 in 1 CARTON | LOTION | 1 | | 6 |
| 70319-220-01 | COSRX | 50 mL in 1 TUBE | LOTION | 50 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70319-220 | COSRX (VITAMIN E VITALIZING SUNSCREEN) LOTION [COSRX INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250523_daf0291e-770c-eaf2-e053-2a95a90a0b67.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70319-220-01 | 70319022001 | 1 TUBE in 1 CARTON (70319-220-01) / 50 mL in 1 TUBE | 1 tube | 2025-12-01 | 0000-00-00 | No | No | Current |