Kenaf wet wipe
- Product NDC
- 72944-0001
- 11-digit product format
- 729440001
- Labeler code
- 72944
- Product ID
- 72944-0001_384bb90a-444d-547a-e063-6394a90a354b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- MEDICELL BIO CO., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-04-09
- Substance
- ALLANTOIN
- Active strength
- .05 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kenaf wet wipe
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .05 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72944-0001-1 | Kenaf wet wipe | 190 g in 1 POUCH | LIQUID | 190 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72944-0001 | KENAF WET WIPE (ALLANTOIN) LIQUID [MEDICELL BIO CO., LTD.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20230210_860f9cc5-a00e-7ccf-e053-2a91aa0a0782.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72944-0001-1 | 72944000101 | 190 g in 1 POUCH (72944-0001-1) | 190 g | 2017-04-09 | 0000-00-00 | No | No | Current |