TRIDERMA CLEAN SOOTHE BOTTOM WASH- bottom wash liquid

TriDerma Clean Soothe Bottom Wash by

Drug Labeling and Warnings

TriDerma Clean Soothe Bottom Wash by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzethonium Chloride 0.12%

PURPOSE

Antiseptic

INDICATIONS & USAGE

Prevents skin infection, removes germs

WARNINGS

for external use only

WHEN USING

keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

Spray directly onto soiled skin. Remove feces or urine. Next, spray onto a clean, soft cloth and gently wipe off remaining residue. Spray again and pat dry.

STORAGE AND HANDLING

store at room temperature. use on children 12 & up and adults

INACTIVE INGREDIENT

Allantoin, Aloe Barbadensis (Aloe Vera) Leaf Juice†, Caprylyl/Capryl Glucoside, Cetyl Hydroxyethylcellulose, Citric Acid, Citrus Aurantium Dulcis Fruit Extract, Cocamidopropyl Betaine, Cocamidopropyl Hydroxysultaine, Decyl Glucoside, Disodium 2-Sulfolaurate, Fragrance/Parfum, Leuconostoc /Radish Root Ferment Filtrate, Lycium Chinensis Fruit Extract, Niacinamide, Olea Europaea Fruit Extract, Opuntia Ficus-Indica Fruit Extract, Panthenol, Potassium Sorbate, Propanediol, Sodium Citrate, Sodium Lauryl Sulfoacetate, Sodium Methyl 2-Sulfolaurate, Tetrasodium Glutamate Diacetate, Water/Aqua, Zinc PCA.

† Certified Organic Ingredient - Mayacert Certifier

KEEP OUT OF REACH OF CHILDREN

If swallowed get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRIDERMA CLEAN SOOTHE BOTTOM WASH 
bottom wash liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-096
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.0012 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-096-88	243 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2025

Labeler - Genuine Virgin Aloe Corporation (961374147)

Registrant - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-096)