Replenix Sunscreen
- Product NDC
- 51326-220
- 11-digit product format
- 513260220
- Labeler code
- 51326
- Product ID
- 51326-220_82ab1eb2-c229-4d32-b2ce-6c837ce4cc57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Topiderm, Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-10-16
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 75; 145 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Replenix Sunscreen
- Brand name suffix
- SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 75 mg/g |
| ZINC OXIDE | 145 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51326-220-01 | Replenix Sunscreen SPF 50 | 63 g in 1 BOTTLE | LOTION | 63 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51326-220 | REPLENIX SUNSCREEN SPF 50 (ZINC OXIDE) LOTION [TOPIDERM, INC.] | 1 | Current NDC, 1 package rows | 20240518_9223ffa8-7af3-4407-9170-482afec536d8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51326-220-01 | 51326022001 | 63 g in 1 BOTTLE (51326-220-01) | 63 g | 2021-10-16 | No | No | Current |