911
- Product NDC
- 61328-120
- 11-digit product format
- 613280120
- Labeler code
- 61328
- Product ID
- 61328-120_471aac11-1c14-86fa-e063-6294a90a082e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Skinfix, Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-26
- Substance
- ALLANTOIN
- Active strength
- .5 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
- 911
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
| Rxcui | 1044541 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61328-120-11 | 911 | 50 g in 1 TUBE | OINTMENT | 50 | | 7 |
| 61328-120-12 | 911 | 8.5 g in 1 TUBE | OINTMENT | 8.5 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61328-120 | 911 (ALLANTOIN) OINTMENT [SKINFIX, INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241228_f28c251e-a91b-4ed4-8224-b47c345f982f.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 |
|---|
| 61328-120-11 | 61328012011 | 50 g in 1 TUBE (61328-120-11) | 50 g | 2018-12-26 | 0000-00-00 | No | No | Current |
| 61328-120-12 | 61328012012 | 8.5 g in 1 TUBE (61328-120-12) | 8.5 g | 2018-12-26 | 0000-00-00 | No | No | Current |
| 61328-120-13 | 61328012013 | 102 g in 1 TUBE (61328-120-13) | 102 g | 2019-05-17 | 0000-00-00 | No | No | Current |