Sulfur Spot Treatment
- Product NDC
- 70707-440
- 11-digit product format
- 707070440
- Labeler code
- 70707
- Product ID
- 70707-440_28da58df-4226-e6db-e063-6394a90aced8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Face Reality, Inc
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-08
- Substance
- SULFUR
- Active strength
- 60 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
- Sulfur Spot Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 60 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 2273805 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70707-440-04 | Sulfur Spot Treatment | 118 mL in 1 BOTTLE | GEL | 118 | | 4 |
| 70707-440-15 | Sulfur Spot Treatment | 44 mL in 1 TUBE | GEL | 44 | | 4 |
| 70707-440-15 | Sulfur Spot Treatment | 1 in 1 BOX | GEL | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70707-440 | SULFUR SPOT TREATMENT (SULFUR) GEL [FACE REALITY, INC] | 4 | Current NDC, Legacy NDC, 3 package rows | 20241210_921e948d-a8c7-4527-9257-4b91dee8fcff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70707-440-04 | 70707044004 | 118 mL in 1 BOTTLE (70707-440-04) | 118 ml | 2020-01-15 | 0000-00-00 | No | No | Current |
| 70707-440-15 | 70707044015 | 1 TUBE in 1 BOX (70707-440-15) / 44 mL in 1 TUBE | 1 tube | 2020-01-08 | 0000-00-00 | No | No | Current |