BiteMD External Analgesic First Aid Antiseptic

Product NDC
79364-0932
11-digit product format
793640932
Labeler code
79364
Product ID
79364-0932_27c08d01-85c1-4961-91bb-70ee991c7827
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine, Camphor (Synthetic), and Phenol
Dosage form
LIQUID
Route
TOPICAL
Labeler
United Industries Corporation
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-01
Substance
BENZOCAINE; CAMPHOR (SYNTHETIC); PHENOL
Active strength
.0524; .03144; .01572 mg/mL; mg/mL; 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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
BiteMD External Analgesic First Aid Antiseptic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE.0524 mg/mL
CAMPHOR (SYNTHETIC).03144 mg/mL
PHENOL.01572 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5, 5TJD82A1ET, 339NCG44TV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79364-0932-1BiteMD External Analgesic First Aid Antiseptic14.7 mL in 1 BOTTLELIQUID14.73

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79364-0932BITEMD EXTERNAL ANALGESIC FIRST AID ANTISEPTIC (BENZOCAINE, CAMPHOR (SYNTHETIC), AND PHENOL) LIQUID [UNITED INDUSTRIES CORPORATION]3Current NDC, Legacy NDC, 1 package rows20250101_4c60db03-6d2b-4ae0-a200-718b3a50eb0f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79364-0932-17936409320114.7 mL in 1 BOTTLE (79364-0932-1) 14.7 ml2020-01-010000-00-00NoNoCurrent