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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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 |
|---|---|
| BENZOCAINE | 200 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| U3RSY48JW5 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 308657 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| eebc03ba-f849-4e70-a653-834f383b6aa4 | Available on FDA.report |
DailyMed Package Descriptions#
| 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 | 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 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sensitive Whitening Tooth-paste | POTASSIUM NITRATE, SODIUM FLUORIDE | Meijer, Inc. | c25b6a95-e604-48e3-bc55-595969d1ce9b | 2025-12-23 | Warnings | M022 |
| parodontax Active Gum Repair | STANNOUS FLUORIDE | Haleon US Holdings LLC | b51ccdd9-c0af-4caa-ad97-ad1d1423b76b | 2025-12-22 | Warnings | M022 |
| parodontax Complete Protection | STANNOUS FLUORIDE | Haleon US Holdings LLC | 59bb84d6-6fd3-4586-bccf-7dc45cbbb39c | 2025-12-22 | Warnings | M022 |
| parodontax Complete Protection | STANNOUS FLUORIDE | Haleon US Holdings LLC | f6912712-ce9b-44aa-8953-b9a8d420f458 | 2025-12-22 | Warnings | M022 |
| parodontax Active Gum Repair Whitening | STANNOUS FLUORIDE | Haleon US Holdings LLC | 817e804c-e55e-4d77-9ab9-ff54ae794725 | 2025-12-22 | Warnings | M022 |
| parodontax Active Gum Repair Breath Freshener | STANNOUS FLUORIDE | Haleon US Holdings LLC | addcb1e2-24b9-4367-adf3-6806e2439a80 | 2025-12-22 | Warnings | M022 |
| parodontax | STANNOUS FLUORIDE | Haleon US Holdings LLC | 0f07aa1a-97be-44af-92d8-a10777e24e0a | 2025-12-22 | Warnings | M022 |
| R B one | PHOSPHATIDYLSERINE, ZINC OXIDE | NPG Bio Pharmaceuticals Co.,Ltd. | 410c40fd-cf94-0301-e063-6294a90ae2de | 2025-12-18 | Warnings | M022 |
| Dem Zero | PHOSPHATIDYLSERINE, MAGNESIUM OXIDE | NPG Bio Pharmaceuticals Co.,Ltd. | 411f1a0f-ed02-cc78-e063-6394a90a0aec | 2025-12-18 | Warnings | M022 |
| Res B one | PHOSPHATIDYLSERINE, ZINC OXIDE | NPG Bio Pharmaceuticals Co.,Ltd. | 21469f58-1d70-774f-e063-6294a90af039 | 2025-12-18 | Warnings | M022 |
| Alzh L | PHOSPHATIDYLSERINE, MAGNESIUM OXIDE | NPG Bio Pharmaceuticals Co.,Ltd. | 41056de0-aaa2-01bb-e063-6394a90af7b8 | 2025-12-18 | Warnings | M022 |
| Lemon | GLYCERIN | TwinMed LLC | fc88eec0-c66c-5d6d-e053-6294a90a13d2 | 2025-12-18 | Warnings | M022 |
| CloSYS | HYDROGEN PEROXIDE | Rowpar Pharmaceuticals, Inc. | 299fc7b1-af6d-4bf9-810f-d35283423fe2 | 2025-12-17 | Warnings | M022 |
| Ipana 20% Benzocaine Topical | BENZOCAINE | Maxill Inc. | c13761e0-d45d-4e0f-ac41-428e005f96bb | 2025-12-17 | Warnings | M022 |
| Ipana 20% Benzocaine Topical | BENZOCAINE | Maxill Inc. | 6dca566b-cb6a-43c4-b6e2-f2bad77fb932 | 2025-12-17 | Warnings | M022 |
| Ipana 20% Benzocaine Topical | BENZOCAINE | Maxill Inc. | f36bb9bd-e9bc-4f35-a388-e0ffadbce6ab | 2025-12-17 | Warnings | M022 |
| Ipana 20% Benzocaine Topical | BENZOCAINE | Maxill Inc. | 7ede08e5-2dfe-4183-905d-28d1cea42407 | 2025-12-17 | Warnings | M022 |
| Ipana 20% Benzocaine Topical | BENZOCAINE | Maxill Inc. | 9de36e4f-f966-4a58-b4bf-9ac3b86b3f09 | 2025-12-17 | Warnings | M022 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | CVS PHARMACY, INC | 3b0ad9ac-4920-45a7-b336-dfa7f8d9bdb2 | 2025-12-17 | Warnings | M022 |
| Sore Throat | PHENOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | 9128d59c-6fa9-4358-865a-802257a9bd25 | 2025-12-16 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | PSN | eebc03ba-f849-4e70-a653-834f383b6aa4 | 5 |
| 308657 | benzocaine 200 MG/ML Mucous Membrane Topical Solution | SCD | eebc03ba-f849-4e70-a653-834f383b6aa4 | 5 |
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | SY | eebc03ba-f849-4e70-a653-834f383b6aa4 | 5 |
Packages#
| 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 |