orajel toothache rinse

Generic: benzyl alcohol, zinc chloride

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

Drug Facts

Product Profile

Brand Name orajel toothache rinse
Generic Name benzyl alcohol, zinc chloride
Labeler church & dwight co., inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

benzyl alcohol 2.7 mg/mL, zinc chloride 1.5 mg/mL

Manufacturer
Church & Dwight Co., Inc.

Identifiers & Regulatory

Product NDC 10237-764
Product ID 10237-764_27e7c3b6-5f9a-a7f3-e063-6394a90a02a7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2016-12-01

Pharmacologic Class

Established (EPC)
pediculicide [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10237764
Hyphenated Format 10237-764

Supplemental Identifiers

RxCUI
1865199
UNII
LKG8494WBH 86Q357L16B
NUI
N0000181811

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 toothache rinse (source: ndc)
Generic Name benzyl alcohol, zinc chloride (source: ndc)
Application Number M022 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2.7 mg/mL
  • 1.5 mg/mL
source: ndc
Packaging
  • 236.6 mL in 1 BOTTLE (10237-764-08)
  • 473.2 mL in 1 BOTTLE (10237-764-16)
source: ndc

Packages (2)

10237-764-08 236.6 mL in 1 BOTTLE (10237-764-08) 10237-764-16 473.2 mL in 1 BOTTLE (10237-764-16)

Ingredients (2)

benzyl alcohol (2.7 mg/mL) zinc chloride (1.5 mg/mL)

Linked Drug Pages (1)

Orajel Toothache Rinse ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "27e7c3b6-5f9a-a7f3-e063-6394a90a02a7", "openfda": {"nui": ["N0000181811"], "unii": ["LKG8494WBH", "86Q357L16B"], "rxcui": ["1865199"], "spl_set_id": ["41709710-5392-3119-e054-00144ff88e88"], "pharm_class_epc": ["Pediculicide [EPC]"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236.6 mL in 1 BOTTLE (10237-764-08)", "package_ndc": "10237-764-08", "marketing_start_date": "20161201"}, {"sample": false, "description": "473.2 mL in 1 BOTTLE (10237-764-16)", "package_ndc": "10237-764-16", "marketing_start_date": "20161201"}], "brand_name": "Orajel Toothache Rinse", "product_id": "10237-764_27e7c3b6-5f9a-a7f3-e063-6394a90a02a7", "dosage_form": "LIQUID", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Pediculicide [EPC]"], "product_ndc": "10237-764", "generic_name": "Benzyl Alcohol, Zinc Chloride", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Orajel Toothache Rinse", "active_ingredients": [{"name": "BENZYL ALCOHOL", "strength": "2.7 mg/mL"}, {"name": "ZINC CHLORIDE", "strength": "1.5 mg/mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161201", "listing_expiration_date": "20261231"}