TULA Skincare Go Away Acne Spot Treatment
- Product NDC
- 72296-040
- 11-digit product format
- 722960040
- Labeler code
- 72296
- Product ID
- 72296-040_a52ed291-5333-41fc-9def-3a06490b616d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TULA Skincare Go Away Acne Spot Treatment
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Tula Life LLC
- Application
- part333D
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-12-24
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE
- Active strength
- 5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 72296-040-15 | TULA Skincare Go Away Acne Spot Treatment | 1 in 1 CARTON | LIQUID | 1 | | 5 |
| 72296-040-15 | TULA Skincare Go Away Acne Spot Treatment | 15 g in 1 TUBE | LIQUID | 15 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72296-040 | TULA SKINCARE GO AWAY ACNE SPOT TREATMENT LIQUID [TULA LIFE LLC] | 5 | Legacy NDC, 2 package rows | 20230101_60eeddcc-2a25-4f9e-87ba-3b1182397766.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72296-040-15 | 72296004015 | 1 TUBE in 1 CARTON (72296-040-15) > 15 g in 1 TUBE | 1 tube | 2021-12-24 | 0000-00-00 | No | No | Current |