HUMANE ACNE WASH
- Product NDC
- 73010-900
- 11-digit product format
- 730100900
- Labeler code
- 73010
- Product ID
- 73010-900_097502bf-7222-dd2b-e063-6394a90a7520
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOYL PEROXIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Apprendista, LLC
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 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
- HUMANE ACNE WASH
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 142034 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73010-900-00 | HUMANE ACNE WASH | 237 mL in 1 BOTTLE | LIQUID | 237 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73010-900 | HUMANE ACNE WASH (BENZOYL PEROXIDE) LIQUID [APPRENDISTA, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231114_1d25fb25-a3d2-4c6b-a975-be7b90b70265.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 |
|---|
| 73010-900-00 | 73010090000 | 237 mL in 1 BOTTLE (73010-900-00) | 237 ml | 2019-04-01 | 0000-00-00 | No | No | Current |