DEEP ACNE
- Product NDC
- 68479-240
- 11-digit product format
- 684790240
- Labeler code
- 68479
- Product ID
- 68479-240_3ca4c257-cc4d-48af-91c0-29522e5a1786
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Dermalogica, LLC.
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-12-01
- Substance
- SULFUR
- Active strength
- 5 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DEEP ACNE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 5 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 283392 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68479-240-00 | DEEP ACNE | 2 mL in 1 POUCH | GEL | 2 | | 2 |
| 68479-240-02 | DEEP ACNE | 1 in 1 CARTON | GEL | 1 | | 2 |
| 68479-240-02 | DEEP ACNE | 15 mL in 1 TUBE | GEL | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68479-240 | DEEP ACNE (SULFUR) GEL [DERMALOGICA, LLC.] | 2 | Current NDC, Legacy NDC, 3 package rows | 20250101_d4e9d230-2ee4-4cc7-a7c9-a7dde50b6f40.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 |
|---|
| 68479-240-00 | 68479024000 | 2 mL in 1 POUCH (68479-240-00) | 2 ml | 2022-12-01 | 0000-00-00 | No | No | Current |
| 68479-240-02 | 68479024002 | 1 TUBE in 1 CARTON (68479-240-02) / 15 mL in 1 TUBE | 1 tube | 2022-12-01 | 0000-00-00 | No | No | Current |