What is NDC 10237-782?

10237-782 is the product NDC for Orajel 2X Medicated Gel (oral pain reliever), Benzocaine 200 mg/g; Menthol 2.6 mg/g 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 2X Medicated Gel (Oral Pain Reliever).

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 2X Medicated Gel?

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 2X Medicated Gel NDC 10237-782 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)10237-782Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10237-0782Add 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
10237-782-25	10237078225	1 TUBE in 1 CARTON (10237-782-25) / 7 g in 1 TUBEMarketed from May 23, 2022

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 2X Medicated Gel
Generic name (nonproprietary): oral pain reliever
Active ingredients: Benzocaine — 200 mg/gMenthol — 2.6 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: May 23, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 10237-782_262be295-4eb0-3136-e063-6294a90a7dccSPL ID 262be295-4eb0-3136-e063-6294a90a7dccSPL set ID 262be295-4eaf-3136-e063-6294a90a7dccRxCUI 2117337UNII U3RSY48JW5, L7T10EIP3AUPC 0310310430283
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410237078225 followed by a unit qualifier and the quantity

Package 10237-0782-25. 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 Nov 5, 2024.

Indications (excerpt from the label)

USE for the temporary relief of pain due to toothaches

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10237-782

What is NDC 10237-782?: 10237-782 is the product NDC for Orajel 2X Medicated Gel (oral pain reliever), Benzocaine 200 mg/g; Menthol 2.6 mg/g 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 2X Medicated Gel (Oral Pain Reliever).
What is the active ingredient?: Benzocaine, Menthol.
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 2X Medicated Gel?: 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
Vicks VapoCool SEVERE plus Intense Pain Reliefbenzocaine and menthol	Benzocaine 15 mg/1; Menthol 20 mg/1	LozengeOral	The Procter & Gamble Manufacturing Company	84126-366
HurriCaine Topical Anestheticbenzocaine	Benzocaine 200 mg/g	GelDental, Oral, Periodontal	Beutlich Pharmaceuticals, LLC	0283-0520
HurriCaine Topical Anesthetic Liquidbenzocaine	Benzocaine 200 mg/g	LiquidDental, Oral, Periodontal	Beutlich Pharmaceuticals, LLC	0283-1116
Orajel Rescue Relief Penoral pain reliever	Zinc chloride 1.5 mg/g + 2 more ingredients	GelOral	Church & Dwight Co., Inc.	10237-731
Sensodyne Complete Protectionstannous fluoride	Stannous fluoride 1.1 mg/g	PasteDental	Haleon US Holdings LLC	0135-0573
4x Medicated Toothache and Gum Creambenzocaine	Benzocaine 20 g/100g + 3 more ingredients	CreamOral	HEB	37808-116
Gumsolbenzocaine, zinc chloride	Benzocaine 1.5 g/30mL; Zinc chloride .03 g/30mL	SprayOral	Kramer Novis	52083-714
Oral Pain Reliefbenzocaine	Benzocaine 200 mg/g	GelOral	GERI-CARE PHARMACEUTICAL CORP	57896-139
4x Medicated Toothache and Gum Creambenzocaine	Benzalkonium chloride .13 g/100g + 3 more ingredients	CreamOral	CVS	69842-631
Mouthwashmenthol, methyl salicylate, thymol	Methyl salicylate .6 mg/mL + 3 more ingredients	LiquidOral	Orazen Inc	71927-006
Made by Dentists Enamel Rebuilding Fresh Mintpotassium nitrate, sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.5 mg/g	PasteDental	MADE BY DENTISTS INC	75065-028
Made by Dentists Sensitive and Whitening Fresh Mintpotassium nitrate, sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.5 mg/g	PasteDental	MADE BY DENTISTS INC	75065-029
UltraCare Anesthetic Gelbenzocaine	Benzocaine 200 mg/g	GelDental, Periodontal, Topical	The Bellport Company, Inc. dba Gingi-Pak	10129-071
Ear Wax Removal Aid Dropscarbamide peroxide	Carbamide peroxide 65 mg/mL	LiquidAuricular (Otic)	BETTER LIVING BRANDS, LLC	21130-793
Sore Throat Relief Cherryphenol	Phenol 1.4 g/100mL	SprayOral	Best Choice (Valu Merchandisers Company)	63941-376
Antiseptic Lil Drug Store Productseucalyptol, menthol, unspecified form, methyl salicylate, and thymol	Eucalyptol .92 mg/mL + 3 more ingredients	LiquidOral	Lil' Drug Store Products, Inc	66715-6861
Benzo-Jelbenzocaine	Benzocaine 200 mg/g	GelDental	Henry Schein Inc.	0404-0033
Kroger Enamel Protection Sensitive Gentle Whiteningpotassium nitrate, sodium fluoride	Potassium nitrate 5 g/100g; Sodium fluoride .15 g/100g	Paste, DentifriceDental	Kroger Company	30142-362
equate Sensitivepotassium nitrate, sodium fluoride	Potassium nitrate 5 g/100g; Sodium fluoride .15 g/100g	Paste, DentifriceDental	Wal-Mart Stores Inc	49035-257
LISTERINE Original Antisepticeucalyptol, menthol, unspecified form, methyl salicylate, and thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Kenvue Brands LLC	69968-0400

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Orajel 2X Medicated Gel (Oral pain reliever) NDC 10237-782