Home NDC 55910-660 DG 4x Medicated Tooth and Gum Cream
Product NDC 55910-660
11-digit product format 559100660
Labeler code 55910
Product ID 55910-660_441d3a38-e992-2d1d-e063-6394a90ae911
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form CREAM
Route ORAL
Labeler Dollar General
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-10-28
Substance ZINC CHLORIDE; BENZALKONIUM CHLORIDE; MENTHOL, UNSPECIFIED FORM; BENZOCAINE
Active strength .15; .13; .26; 20 g/100g; g/100g; g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 55910-660 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 55910-660 55910-660-09 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 DG 4x Medicated Tooth and Gum Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC CHLORIDE .15 g/100g BENZALKONIUM CHLORIDE .13 g/100g MENTHOL, UNSPECIFIED FORM .26 g/100g BENZOCAINE 20 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2370903 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55910-660-09 DG 4x Medicated Tooth and Gum Cream 9.4 g in 1 TUBE CREAM 9.4 6 55910-660-09 DG 4x Medicated Tooth and Gum Cream 1 in 1 CARTON CREAM 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-660 DG 4X MEDICATED TOOTH AND GUM CREAM (BENZOCAINE) CREAM [DOLLAR GENERAL] 4 Current NDC, Legacy NDC, 2 package rows 20250413_b2c156f0-6d11-1eba-e053-2995a90a6db8.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 55910-660-09 55910066009 1 TUBE in 1 CARTON (55910-660-09) / 9.4 g in 1 TUBE 1 tube 2020-10-28 0000-00-00 No No Current