What is NDC 10237-731?

10237-731 is the product NDC for Orajel Rescue Relief Pen (oral pain reliever), Zinc chloride 1.5 mg/g + 2 more ingredients gel, listed with the FDA by Church & Dwight Co., Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Orajel Rescue Relief Pen (Oral Pain Reliever).

What is the active ingredient?

Zinc chloride, Menthol, Benzocaine.

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 Rescue Relief Pen?

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 Rescue Relief Pen NDC 10237-731

NDC codes

FDA NDC Directory

Product NDC (as listed)10237-731Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10237-0731Add 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
10237-731-07	10237073107	1 APPLICATOR in 1 BLISTER PACK (10237-731-07) / 2 g in 1 APPLICATORMarketed from Feb 1, 2025
10237-731-27	10237073127	2 BLISTER PACK in 1 PACKAGE (10237-731-27) / 1 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATORMarketed from Jun 1, 2025

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 Rescue Relief Pen
Generic name (nonproprietary): oral pain reliever
Active ingredients: Zinc chloride — 1.5 mg/gMenthol — 2.6 mg/gBenzocaine — 200 mg/g
Dosage form: Gel
Route: Oral
Labeler: Church & Dwight Co., Inc.NDC labeler code 10237
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 022
Marketing start: Feb 1, 2025
Listing expires: Dec 31, 2026
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 10237-731_38d791e8-33d3-22e4-e063-6394a90aff90SPL ID 38d791e8-33d3-22e4-e063-6394a90aff90SPL set ID 2d68eec5-ae8a-9cdf-e063-6294a90a9799RxCUI 2362013UNII 86Q357L16B, L7T10EIP3A, U3RSY48JW5
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410237073107 followed by a unit qualifier and the quantity

Package 10237-0731-07. 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 Jun 1, 2025.

Indications (excerpt from the label)

USES • 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 10237-731

What is NDC 10237-731?: 10237-731 is the product NDC for Orajel Rescue Relief Pen (oral pain reliever), Zinc chloride 1.5 mg/g + 2 more ingredients gel, listed with the FDA by Church & Dwight Co., Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Orajel Rescue Relief Pen (Oral Pain Reliever).
What is the active ingredient?: Zinc chloride, Menthol, Benzocaine.
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 Rescue Relief Pen?: 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
Alpha-Caine Topical Anestheticbenzocaine	Benzocaine 200 mg/g	GelDental, Periodontal	Dental Technologies, Inc.	55346-2903
LISTERINE Original Antisepticeucalyptol, menthol, unspecified form, methyl salicylate, and thymol	Eucalyptol .92 mg/mL + 3 more ingredients	MouthwashOral	Kenvue Brands LLC	69968-0400
Lolleez Watermelonpectin	Pectin 11.5 mg/7g	LozengeOral	BFY LLC	72427-3295
meijer Sensitive FRESH MINTpotassium nitrate, sodium fluoride	Potassium nitrate 5 g/100g; Sodium fluoride .24 g/100g	Paste, DentifriceDental	Meijer, Inc.	79481-0039
parodontax Active Gum Repair Whiteningstannous fluoride	Stannous fluoride 1.1 mg/g	PasteDental	Haleon US Holdings LLC	0135-0638
Opalescence Sensitivity Relief Whiteningpotassium nitrate and sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.1 mg/g	Gel, DentifriceDental	Ultradent Products, Inc.	51206-308
Sensitivity Relief Fluoride Freepotassium nitrate	Potassium nitrate 50 mg/g	Paste, DentifriceDental	Health and Natural Beauty USA Corp	63404-2105
Sucrets Sore Throat Wild Cherrydyclonine hydrochloride	Dyclonine hydrochloride 2 mg/1	LozengeOral	Insight Pharmaceuticals LLC	63736-560
BencoCaine Topical Anestheticbenzocaine	Benzocaine 200 mg/g	GelDental	Benco Dental	66975-356
Lemon Glyceringlycerin	Glycerin .3 g/4g	SwabOral	Dynarex Corporation	67777-161
Anesgerm LA MUELA Fast Pain Reliefbenzocaine 20%	Benzocaine 200 mg/mL	LiquidTopical	Germa Products, LLC	73635-7101
SENSODYNE PRONAMEL Intensive Enamel Repair Extra Freshpotassium nitrate and sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.15 mg/g	PasteOral	Haleon US Holdings LLC	0135-0486
UltraCare Anesthetic Gelbenzocaine	Benzocaine 200 mg/g	GelDental, Periodontal, Topical	The Bellport Company, Inc. dba Gingi-Pak	10129-071
Opal by Opalescence Sensitivitypotassium nitrate and sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 1.1 mg/g	Gel, DentifriceDental	Ultradent Products, Inc.	51206-311
Alpha-Caine Topical Anestheticbenzocaine	Benzocaine 200 mg/g	GelDental, Periodontal	Dental Technologies, Inc.	55346-2901
Sensitivity and Gum with Cavity Protectionpotassium nitrate and sodium fluoride	Potassium nitrate 50 mg/g; Sodium fluoride 7.6 mg/g	Paste, DentifriceDental	Health and Natural Beauty USA Corp	63404-2210
Sucretsdyclonine hcl, menthol, and pectin	Dyclonine hydrochloride 2 mg/1 + 2 more ingredients	LozengeOral	Insight Pharmaceuticals LLC	63736-567
BencoCaine Topical Anestheticbenzocaine	Benzocaine 200 mg/g	GelDental	Benco Dental	66975-357
Sore Mouth Cleanserhydrogen peroxide	Hydrogen peroxide 150 mg/10mL	MouthwashTopical	CVS Pharmacy, Inc.	69842-008
Lolleez Variety Packpectin	Pectin 11.5 mg/7g	LozengeOral	BFY LLC	72427-3195

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Orajel Rescue Relief Pen (Oral pain reliever) NDC 10237-731