What is NDC 10157-2127?

10157-2127 is the product NDC for Kanka Triple Action, Benzocaine 20 g/100g; Menthol, Unspecified form 2 g/100g gel, listed with the FDA by Blistex Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Kanka Triple Action (BENZOCAINE and MENTHOL, UNSPECIFIED FORM).

What is the active ingredient?

Benzocaine, Menthol, Unspecified form.

Blistex Inc., NDC labeler code 10157. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Kanka Triple Action?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Kanka Triple Action NDC 10157-2127

NDC codes

FDA NDC Directory

Product NDC (as listed)10157-2127Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10157-2127Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
10157-2127-1	1015721270110157212701	1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBEMarketed from Jan 6, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Kanka Triple Action
Generic name (nonproprietary): benzocaine and menthol, unspecified form
Active ingredients: Benzocaine — 20 g/100gMenthol, Unspecified form — 2 g/100g
Dosage form: Gel
Route: Oral
Labeler: Blistex Inc.NDC labeler code 10157
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 022
Marketing start: Jan 6, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 10157-2127_225703ba-c471-4c9a-9c01-4b7f075b7878SPL ID 225703ba-c471-4c9a-9c01-4b7f075b7878SPL set ID 078fcdab-38a1-4a9a-bdd3-e17446591ea8RxCUI 1006079UNII U3RSY48JW5, L7T10EIP3AUPC 0041388013145
Pharmacologic class: Standardized Chemical Allergen

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410157212701 followed by a unit qualifier and the quantity

Package 10157-2127-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 9, 2025.

Indications (excerpt from the label)

Uses for the temporary relief of pain associated with canker sores, minor irritation of the mouth and gums caused by dentures or orthodontic appliances, or minor injury of the mouth or gums.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10157-2127

What is NDC 10157-2127?: 10157-2127 is the product NDC for Kanka Triple Action, Benzocaine 20 g/100g; Menthol, Unspecified form 2 g/100g gel, listed with the FDA by Blistex Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Kanka Triple Action (BENZOCAINE and MENTHOL, UNSPECIFIED FORM).
What is the active ingredient?: Benzocaine, Menthol, Unspecified form.
Who is the labeler?: Blistex Inc., NDC labeler code 10157. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Kanka Triple Action?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 022

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 022
Product	Strength	Form · route	Labeler	Product NDC
Hydrogen Peroxide 3 Percent ReadyInCasehydrogen peroxide	Hydrogen peroxide 3 mL/100mL	LiquidTopical	P & L Development, LLC	49580-0268
Salinenasal	Sodium chloride 6.5 mg/mL	SprayNasal	Bi-Mart	37835-998
CVS Health Sensitive Enamel Repairsodium fluoride	Sodium fluoride .15 g/100g; Potassium nitrate 5 g/100g	Paste, DentifriceOral	CVS	51316-169
Ricola Max Nasal Care Cool Mentholmenthol	Menthol 15.3 mg/1	LozengeOral	Ricola Ag	54305-206
Orajel Medicated for Toothache and Gum, Liquidbenzocaine and menthol	Benzocaine 200 mg/mL; Menthol, Unspecified form 1 mg/mL	LiquidTopical	Church & Dwight Co., Inc.	10237-796
Throat Balm Caramel Pectinpectin	Pectin 3.8 mg/1	LozengeOral	Ricola Ag	54305-301
Throat Balm Caramel Pectinpectin	Pectin 3.8 mg/1	LozengeOral	Ricola USA Inc.	63667-301
Hydrogen Peroxide 3 Percenthydrogen peroxide	Hydrogen peroxide 2.65 mL/100mL	LiquidTopical	Whole Foods Market	42681-6414
Sore throat cherryphenol	Phenol 1.4 g/100mL	SprayOral	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	55910-376
Crest Pro-Health Gum DetoxifyWinter Mintcetylpyridinium chloride	Cetylpyridinium chloride .07 g/mL	RinseOral	The Procter & Gamble Manufacturing Company	84126-648
Crest Kids Advanced Color Changingsodium monofluorophosphate	Sodium monofluorophosphate 1.6 mg/g	Paste, DentifriceDental	Procter & Gamble Manufactura, S de R.L. de C.V.	58933-012
Sootheez Berry Lemonadepectin	Pectin 11.5 mg/3.5g	LozengeOral	BFY LLC	72427-4014
Sootheez Organic Wild Cherrypectin	Pectin 11.5 mg/3.5g	LozengeOral	BFY LLC	72427-3714
Quality Choice Oral Pain Reliefbenzocaine 20%, benzalkonium chloride 1%	Benzocaine 200 mg/g; Benzalkonium chloride 10 mg/g	GelTopical	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	83324-035
Rite Aid Professional Strengthbenzocaine	Benzocaine 20 g/100g	LiquidOral	Rite Aid	11822-5340
SENSODYNE Rapid Reliefstannous fluoride	Stannous fluoride 1.1 mg/g	PasteOral	Haleon US Holdings LLC	0135-0622
Iodent Oral Analgesicbenzocaine	Benzocaine 200 mg/g	GelTopical	United Exchange Corp.	65923-094
Sootheez Organic Wild Cherrypectin	Pectin 11.5 mg/3.5g	LozengeOral	BFY LLC	72427-3714
Topcare Sore Throat Menthol Flavorphenol	Phenol 1.4 g/100mL	SprayOral	TOPCO ASSOCIATES LLC	36800-606
Sensodyne Pronamel Gentle Whitening Advancedpotassium nitrate and sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.15 mg/g	PasteDental	Haleon US Holdings LLC	0135-0580

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Kanka Triple Action (Benzocaine and menthol, unspecified form) NDC 10157-2127