Rexall

Product NDC
55910-346
11-digit product format
559100346
Labeler code
55910
Product ID
55910-346_3c30c101-f57c-f3ba-e063-6394a90ac007
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
LIQUID
Route
ORAL
Labeler
Rexall
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2015-01-01
Substance
BENZOCAINE
Active strength
20 g/100mL
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
Rexall
Brand name suffix
Maximum Strength
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE20 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5
Rxcui308657

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55910-346-79RexallMaximum Strength14.7 mL in 1 BOTTLELIQUID14.711
55910-346-79RexallMaximum Strength1 in 1 CARTONLIQUID111

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BENZOCAINEACTIVE INGREDIENTU3RSY48JW5REXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
BENZOCAINEACTIVE MOIETYU3RSY48JW5REXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
BENZYL ALCOHOLINACTIVE INGREDIENTLKG8494WBHREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3REXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TYREXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-346REXALL MAXIMUM STRENGTH (BENZOCAINE) LIQUID [REXALL]10Current NDC, Legacy NDC, 2 package rows20250119_8f6e2780-cfb7-4bef-9b7d-13cb80d8923e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308657benzocaine 20 % Mucous Membrane Topical SolutionPSN8f6e2780-cfb7-4bef-9b7d-13cb80d8923e11
308657benzocaine 200 MG/ML Mucous Membrane Topical SolutionSCD8f6e2780-cfb7-4bef-9b7d-13cb80d8923e11
308657benzocaine 20 % Mucous Membrane Topical SolutionSY8f6e2780-cfb7-4bef-9b7d-13cb80d8923e11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55910-346-69559100346691 BOTTLE in 1 CARTON (55910-346-69) > 14.7 mL in 1 BOTTLE (55910-346-61) 1 bottle2015-01-130000-00-00NoNoCurrent
55910-346-79559100346791 BOTTLE in 1 CARTON (55910-346-79) / 14.7 mL in 1 BOTTLE1 bottle2023-02-01NoNoHistorical