orajel rescue relief pen

Generic: oral pain reliever

Labeler: church & dwight co., inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name orajel rescue relief pen
Generic Name oral pain reliever
Labeler church & dwight co., inc.
Dosage Form GEL
Routes
ORAL
Active Ingredients

benzocaine 200 mg/g, menthol 2.6 mg/g, zinc chloride 1.5 mg/g

Manufacturer
Church & Dwight Co., Inc.

Identifiers & Regulatory

Product NDC 10237-731
Product ID 10237-731_38d791e8-33d3-22e4-e063-6394a90aff90
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2025-02-01

Pharmacologic Class

Established (EPC)
standardized chemical allergen [epc]
Chemical Structure
allergens [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10237731
Hyphenated Format 10237-731

Supplemental Identifiers

RxCUI
2362013
UNII
U3RSY48JW5 L7T10EIP3A 86Q357L16B
NUI
N0000185508 N0000175629 N0000184306 M0000728

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name orajel rescue relief pen (source: ndc)
Generic Name oral pain reliever (source: ndc)
Application Number M022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/g
  • 2.6 mg/g
  • 1.5 mg/g
source: ndc
Packaging
  • 1 APPLICATOR in 1 BLISTER PACK (10237-731-07) / 2 g in 1 APPLICATOR
  • 2 BLISTER PACK in 1 PACKAGE (10237-731-27) / 1 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR
source: ndc

Packages (2)

Ingredients (3)

benzocaine (200 mg/g) menthol (2.6 mg/g) zinc chloride (1.5 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38d791e8-33d3-22e4-e063-6394a90aff90", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["U3RSY48JW5", "L7T10EIP3A", "86Q357L16B"], "rxcui": ["2362013"], "spl_set_id": ["2d68eec5-ae8a-9cdf-e063-6294a90a9799"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 BLISTER PACK (10237-731-07)  / 2 g in 1 APPLICATOR", "package_ndc": "10237-731-07", "marketing_start_date": "20250201"}, {"sample": false, "description": "2 BLISTER PACK in 1 PACKAGE (10237-731-27)  / 1 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR", "package_ndc": "10237-731-27", "marketing_start_date": "20250601"}], "brand_name": "Orajel Rescue Relief Pen", "product_id": "10237-731_38d791e8-33d3-22e4-e063-6394a90aff90", "dosage_form": "GEL", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "10237-731", "generic_name": "Oral Pain Reliever", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Orajel Rescue Relief Pen", "active_ingredients": [{"name": "BENZOCAINE", "strength": "200 mg/g"}, {"name": "MENTHOL", "strength": "2.6 mg/g"}, {"name": "ZINC CHLORIDE", "strength": "1.5 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}