Anesgerm LA MUELA

Product NDC
73635-7101
11-digit product format
736357101
Labeler code
73635
Product ID
73635-7101_40d07e93-4ae8-9c91-e063-6394a90ac00a
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine 20%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Germa Products, LLC
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-03-29
Substance
BENZOCAINE
Active strength
200 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

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct73635-7101DDiscontinued by firm2026-07-31
excluded packagepackage73635-710173635-7101-5DDiscontinued by firm2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Anesgerm LA MUELA Fast Pain ReliefBENZOCAINE 20%Germa Products, LLCbf7842a2-9c0b-3fc3-e053-2995a90a36c12025-10-10WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warning Warnings: Do not exceed recommended dosage. Keep out of reach of children. In case of overdose, get medical help immediately. Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before.

Additional Listing Data#

Finished product
Yes
Brand name base
Anesgerm LA MUELA
Brand name suffix
Fast Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE200 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5
Rxcui308657

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73635-7101-5Anesgerm LA MUELAFast Pain Relief14.8 mL in 1 BOTTLE, WITH APPLICATORLIQUID14.86
73635-7101-5Anesgerm LA MUELAFast Pain Relief1 in 1 BOXLIQUID16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73635-7101ANESGERM LA MUELA FAST PAIN RELIEF (BENZOCAINE 20%) LIQUID [GERMA PRODUCTS, LLC]4Current NDC, Legacy NDC, 2 package rows20241017_bf7842a2-9c0b-3fc3-e053-2995a90a36c1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308657benzocaine 20 % Mucous Membrane Topical SolutionPSNbf7842a2-9c0b-3fc3-e053-2995a90a36c16
308657benzocaine 200 MG/ML Mucous Membrane Topical SolutionSCDbf7842a2-9c0b-3fc3-e053-2995a90a36c16
308657benzocaine 20 % Mucous Membrane Topical SolutionSYbf7842a2-9c0b-3fc3-e053-2995a90a36c16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73635-7101-5736357101051 BOTTLE, WITH APPLICATOR in 1 BOX (73635-7101-5) / 14.8 mL in 1 BOTTLE, WITH APPLICATOR2019-03-290000-00-00NoNoCurrent