10237-118 NDC - TOUCHLAND HELLO KITTY POWER MIST HAND SANITIZER BERRY BLISS (ALCOHOL)

Drug Information

  • Product NDC: 10237-118
  • Proprietary Name: Touchland Hello Kitty Power Mist Hand Sanitizer Berry Bliss
  • Non Proprietary Name: ALCOHOL
  • Active Ingredient(s): 70 mL/100mL ALCOHOL
  • Administration Route(s): TOPICAL
  • Dosage Form(s): SPRAY

Labeler Information

Field Name Field Value
Labeler Name: Church & Dwight Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: 505G(a)(3)
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:8/1/2024

Package Information

No. Package Code Package Description Billing Unit
110237-118-011 POUCH in 1 CASE (10237-118-01) / 1 BOTTLE, SPRAY in 1 POUCH / 30 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC10237-118The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMETouchland Hello Kitty Power Mist Hand Sanitizer Berry BlissThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEALCOHOLThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/1/2024Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBER505G(a)(3)The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAMEChurch & Dwight Co., Inc.The translation of the dosage form Code submitted by the firm.
SUBSTANCE NAMEALCOHOLThe translation of the route code submitted by the firm, indicating route of administration.
ACTIVE NUMERATOR STRENGTH70 
ACTIVE INGRED UNITmL/100mL 

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This page was last updated on: 9/11/2026

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