Package 10237-731-07

Brand: orajel rescue relief pen

Generic: oral pain reliever
NDC Package

Package Facts

Identity

Package NDC 10237-731-07
Digits Only 1023773107
Product NDC 10237-731
Description

1 APPLICATOR in 1 BLISTER PACK (10237-731-07) / 2 g in 1 APPLICATOR

Marketing

Marketing Status
Marketed Since 2025-02-01
Brand orajel rescue relief pen
Generic oral pain reliever
Sample Package No

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"}