Sooth-a-Sting

Product NDC
50332-0050
11-digit product format
503320050
Labeler code
50332
Product ID
50332-0050_4ca45a41-0ec1-49fa-adc2-4cc3453120a9
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
SWAB
Route
TOPICAL
Labeler
HART Health
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2000-01-01
Substance
BENZOCAINE; MENTHOL, UNSPECIFIED FORM
Active strength
.12; .006 g/.6mL; g/.6mL
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
Sooth-a-Sting
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE.12 g/.6mL
MENTHOL, UNSPECIFIED FORM.006 g/.6mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5, L7T10EIP3A
Rxcui1037117

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50332-0050SOOTH-A-STING (BENZOCAINE) SWAB [HART HEALTH]3Current NDC, Legacy NDC20240119_bd7229b6-813a-4149-bfe2-fe682f270ff4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1037117benzocaine 20 % / menthol 1 % Medicated PadPSNbd7229b6-813a-4149-bfe2-fe682f270ff43
1037117benzocaine 200 MG/ML / menthol 10 MG/ML Medicated PadSCDbd7229b6-813a-4149-bfe2-fe682f270ff43
1037117benzocaine 20 % / menthol 1 % Topical SwabSYbd7229b6-813a-4149-bfe2-fe682f270ff43

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50332-0050-05033200500010 AMPULE in 1 BOX (50332-0050-0) / .6 mL in 1 AMPULE10 ampule2000-01-010000-00-00NoNoCurrent
50332-0050-450332005004100 AMPULE in 1 BAG (50332-0050-4) / .6 mL in 1 AMPULE100 ampule2000-01-010000-00-00NoNoCurrent