Naturium Sulfur Spot Treatment 8%
- Product NDC
- 76354-120
- 11-digit product format
- 763540120
- Labeler code
- 76354
- Product ID
- 76354-120_43961b71-929a-943b-e063-6294a90afd73
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- e.l.f. Cosmetics, Inc
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-17
- Substance
- SULFUR
- Active strength
- 80 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Naturium Sulfur Spot Treatment 8%
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 80 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 2605592 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76354-120-01 | Naturium Sulfur Spot Treatment 8% | 1 in 1 CARTON | LIQUID | 1 | | 3 |
| 76354-120-01 | Naturium Sulfur Spot Treatment 8% | 15 mL in 1 TUBE | LIQUID | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76354-120 | NATURIUM SULFUR SPOT TREATMENT 8% (SULFUR) LIQUID [E.L.F. COSMETICS, INC] | 2 | Current NDC, 2 package rows | 20241212_0a4a9aed-5eeb-f648-e063-6394a90a1d76.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76354-120-01 | 76354012001 | 1 TUBE in 1 CARTON (76354-120-01) / 15 mL in 1 TUBE | 1 tube | 2022-06-17 | No | No | Historical |