Kank-A
- Product NDC
- 10157-9477
- 11-digit product format
- 101579477
- Labeler code
- 10157
- Product ID
- 10157-9477_55568382-5b9f-4bc1-9532-38fb810532d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- LIQUID
- Route
- BUCCAL
- Labeler
- Blistex Inc.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-12-01
- Substance
- BENZOCAINE
- Active strength
- 200 mg/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kank-A
- Brand name suffix
- Mouth Pain
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 200 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 308657 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10157-9477-1 | Kank-A Mouth Pain | 9.75 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9.75 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10157-9477 | KANK-A MOUTH PAIN (BENZOCAINE) LIQUID [BLISTEX INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241220_eebc03ba-f849-4e70-a653-834f383b6aa4.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 |
|---|
| 10157-9477-1 | 10157947701 | 9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1) | 9.75 ml | 2011-12-01 | 0000-00-00 | No | No | Current |