Scrub Care

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 007470579

Effective Date

April 30, 2025

Labeling Type

HUMAN OTC DRUG LABEL

Active Ingredients

Chlorhexidine(2 mg in 100 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

0116-0722

Application Number

NDA019422

Marketing Category

NDA (C73594)

Route of Administration

TOPICAL

Effective Date

April 30, 2025

Ingredients

HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)Inactive

Code: S38J6RZN16Class: IACT

COCO DIETHANOLAMIDEInactive

Code: 92005F972DClass: IACT

WATERInactive

Code: 059QF0KO0RClass: IACT

CITRIC ACID MONOHYDRATEInactive

Code: 2968PHW8QPClass: IACT

Code: MOR84MUD8EClass: ACTIBQuantity: 2 mg in 100 mL

LAURAMINE OXIDEInactive

Code: 4F6FC4MI8WClass: IACT