Cleanslate
- Product NDC
- 75601-1004
- 11-digit product format
- 756011004
- Labeler code
- 75601
- Product ID
- 75601-1004_d56f8ec0-0dab-b4a2-e053-2a95a90a7437
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Punch Studio, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-14
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75601-1004-1 | Cleanslate | 30 mL in 1 BOTTLE, SPRAY | LIQUID | 30 | | 5 |
| 75601-1004-2 | Cleanslate | 1 in 1 BOX | LIQUID | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75601-1004 | CLEANSLATE (ALCOHOL) LIQUID [PUNCH STUDIO, LLC] | 5 | Legacy NDC, 2 package rows | 20220113_b1aa83ed-c721-6239-e053-2a95a90a7e7c.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 |
|---|
| 75601-1004-1 | 75601100401 | 30 mL in 1 BOTTLE, SPRAY | 30 ml | | | | | Historical |
| 75601-1004-2 | 75601100402 | 1 BOTTLE, SPRAY in 1 BOX (75601-1004-2) > 30 mL in 1 BOTTLE, SPRAY (75601-1004-1) | | 2020-10-14 | 0000-00-00 | No | No | Current |