Alcohol Prep Pad
- Product NDC
- 51142-444
- 11-digit product format
- 511420444
- Labeler code
- 51142
- Product ID
- 51142-444_25da293c-7ff5-8fe3-e063-6394a90a9af1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol Prep Pad
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- ASO LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-24
- Substance
- ISOPROPYL ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alcohol Prep Pad
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ISOPROPYL ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ND2M416302 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51142-444-01 | Alcohol Prep Pad | 0.4 mL in 1 POUCH | LIQUID | 0.4 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51142-444 | ALCOHOL PREP PAD LIQUID [ASO LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241103_7481bfb9-2baf-b1ec-e053-2991aa0ad2de.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51142-444-01 | 51142044401 | .4 mL in 1 POUCH (51142-444-01) | 2018-09-24 | 0000-00-00 | No | No | Current |