What is NDC 10237-887?

10237-887 is the product NDC for Orajel 4X Medicated Toothache and Gum, Benzocaine 200 mg/g + 3 more ingredients gel, listed with the FDA by Church & Dwight Co., Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Orajel 4X Medicated Toothache and Gum (Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride).

What is the active ingredient?

Benzocaine, Menthol, Unspecified form, Benzalkonium chloride, Zinc chloride.

Church & Dwight Co., Inc., NDC labeler code 10237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Orajel 4X Medicated Toothache and Gum?

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.

Orajel 4X Medicated Toothache and Gum NDC 10237-887

NDC codes

FDA NDC Directory

Product NDC (as listed)10237-887Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10237-0887Add 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
10237-887-25	1023708872510237088725	1 TUBE in 1 CARTON (10237-887-25) / 7 g in 1 TUBEMarketed from Aug 31, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Orajel 4X Medicated Toothache and Gum
Generic name (nonproprietary): benzalkonium chloride, benzocaine, menthol, zinc chloride
Active ingredients: Benzocaine — 200 mg/gMenthol, Unspecified form — 7.6 mg/gBenzalkonium chloride — .2 mg/gZinc chloride — 1.5 mg/g
Dosage form: Gel
Route: Topical
Labeler: Church & Dwight Co., Inc.NDC labeler code 10237
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 022
Marketing start: Aug 31, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 10237-887_5a1bd621-3a4b-2fa1-e063-6294a90a5b7cSPL ID 5a1bd621-3a4b-2fa1-e063-6294a90a5b7cSPL set ID 5a1b4133-0eac-2f8f-e063-6394a90af8f6RxCUI 2751340UNII U3RSY48JW5, L7T10EIP3A, F5UM2KM3W7, 86Q357L16BUPC 0310310325039
Pharmacologic class: Copper Absorption Inhibitor; 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410237088725 followed by a unit qualifier and the quantity

Package 10237-0887-25. 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 Aug 28, 2026.

Indications (excerpt from the label)

Use first aid to help prevent infection in minor oral irritation for the temporary relief of pain due to minor irritation or injury of the mouth and gums occasional sore mouth and sore throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10237-887

What is NDC 10237-887?: 10237-887 is the product NDC for Orajel 4X Medicated Toothache and Gum, Benzocaine 200 mg/g + 3 more ingredients gel, listed with the FDA by Church & Dwight Co., Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Orajel 4X Medicated Toothache and Gum (Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride).
What is the active ingredient?: Benzocaine, Menthol, Unspecified form, Benzalkonium chloride, Zinc chloride.
Who is the labeler?: Church & Dwight Co., Inc., NDC labeler code 10237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Orajel 4X Medicated Toothache and Gum?: 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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