Avant 70% Alcohol Gel

Product NDC
68306-116
11-digit product format
683060116
Labeler code
68306
Product ID
68306-116_4d4ffa75-38db-5fca-e063-6294a90abb97
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
B4 Soap LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-01-12
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Avant 70% Alcohol Gel
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui581662

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68306-116-01Avant 70% Alcohol Gel208198 mL in 1 DRUMGEL2081983

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68306-116AVANT 70% ALCOHOL GEL (ALCOHOL) GEL [B4 VENTURES LLC]2Current NDC, 1 package rows20231121_241f4334-2e88-4f7b-a0c7-c93da9f5086c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN241f4334-2e88-4f7b-a0c7-c93da9f5086c3
581662ethanol 0.7 ML/ML Topical GelSCD241f4334-2e88-4f7b-a0c7-c93da9f5086c3
581662ethanol 70 % Topical GelSY241f4334-2e88-4f7b-a0c7-c93da9f5086c3
581662ethyl alcohol 70 % Topical GelSY241f4334-2e88-4f7b-a0c7-c93da9f5086c3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68306-116-0168306011601208198 mL in 1 DRUM (68306-116-01) 208198 ml2023-01-12NoNoHistorical