Home NDC 80070-230 Anbesol
Product NDC 80070-230
11-digit product format 800700230
Labeler code 80070
Product ID 80070-230_54dcc1e5-3718-75e8-e063-6294a90ab793
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE
Dosage form SOLUTION
Route TOPICAL
Labeler Foundation Consumer Brands
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-09-15
Substance BENZOCAINE
Active strength 200 mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Anbesol
Brand name suffix Maximum Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308657 Internal RxNorm lookup 608897 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80070-230-41 AnbesolMaximum Strength 12 mL in 1 BOTTLE SOLUTION 12 4 80070-230-41 AnbesolMaximum Strength 1 in 1 BLISTER PACK SOLUTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80070-230 ANBESOL MAXIMUM STRENGTH (BENZOCAINE) SOLUTION [FOUNDATION CONSUMER BRANDS] 4 Current NDC, Legacy NDC, 2 package rows 20250221_8c6ac499-9bd2-4ea5-9f26-df7947bff4a6.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 32 of 40 · 786 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 80070-230-41 80070023041 1 BOTTLE in 1 BLISTER PACK (80070-230-41) / 12 mL in 1 BOTTLE 1 bottle 2021-09-15 0000-00-00 No No Current