Quality Choice

Product NDC
83324-299
11-digit product format
833240299
Labeler code
83324
Product ID
83324-299_414fb186-8272-58da-e063-6394a90a7ac6
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
GEL
Route
TOPICAL
Labeler
Chain Drug Marketing Association, Inc.
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-01
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
U3RSY48JW5BENZOCAINE94-09-7BENZOCAINE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83324-299-42833240299421 TUBE in 1 CARTON (83324-299-42) / 11.9 g in 1 TUBE1 tube2025-10-31NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
QC Maximum Strength Oral Analgesic 0.42oz 95362 (Benzocaine)Chain Drug Marketing Association, Inc.2025-10-16HUMAN OTC DRUG LABEL4
Quality Choice - Chain Drug Marketing Association, Inc.Chain Drug Marketing Association, Inc.2025-03-27HUMAN OTC DRUG LABEL3