Home NDC 10202-853 7 Select Oral Pain Maximum Strength Relief
Product NDC 10202-853
11-digit product format 102020853
Labeler code 10202
Product ID 10202-853_427bbea1-432f-6911-e063-6394a90a9d10
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route TOPICAL
Labeler 7-ELEVEN, INC.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-12-08
Substance BENZOCAINE
Active strength 200 mg/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 7 Select Oral Pain Maximum Strength Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 200 mg/g
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238910 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10202-853-14 7 Select Oral Pain Maximum Strength Relief 14 g in 1 TUBE GEL 14 9 10202-853-14 7 Select Oral Pain Maximum Strength Relief 1 in 1 BLISTER PACK GEL 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10202-853 7 SELECT ORAL PAIN MAXIMUM STRENGTH RELIEF (BENZOCAINE) GEL [7-ELEVEN, INC.] 7 Current NDC, Legacy NDC, 2 package rows 20241222_f170a570-1c50-4b9a-be16-9b01bf5eaa74.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 9 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 10202-853-14 10202085314 1 TUBE in 1 BLISTER PACK (10202-853-14) / 14 g in 1 TUBE 1 tube 2016-12-08 0000-00-00 No No Current