HES CLEAN ADAM- alcohol gel

HES CLEAN ADAM by

Drug Labeling and Warnings

HES CLEAN ADAM by is a Otc medication manufactured, distributed, or labeled by DOCTOR C&C. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Alcohol 3%

INACTIVE INGREDIENT

Inactive ingredients:
Water, Disodium Laureth Sulfosuccinate, Acrylates Copolymer, Hippophae Rhamnoides Fruit Extract, Cocamidopropyl Betaine, TEA-Cocoyl Glutamate, Panax Ginseng Root Extract, Lactobacillus/Soybean Ferment Extract, Salix Alba (Willow) Bark Extract, Cinnamomum Cassia Bark Extract, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Lactuca Indica Extract, Corydalis Ochotensis Extract, Draba Nemorosa Extract, Chenopodium Album Flower Extract, Propylene Glycol,
Triethanolamine, PEG-40 Hydrogenated Castor Oil, Chlorhexidine Digluconate, Caprylyl Glycol, Ethylhexylglycerin, Menthol, Fragrance, Ascorbic Acid

PURPOSE

Purpose: Sanitizer

WARNING

Warning:
1. Always keep out of reach of children
2. Recap the bottle after use
3. Do not keep in hot and cold places and under direct sunlight

KEEP OUT OF REACH OF CHILDREN

Always keep out of reach of children

Product Characteristics

Mild cleansing components softly cover sensitive skin without strains, giving freshness and maintaining cleanliness and neatness for a long time.

Directions for use

Directions for use:
1. If following sympoms appear after use, stop using this product and consult a dermatologist:
1) in case of irritations such as inflammation and swelling during usage
2) in case applied skin shows the same symptoms as 1) in direct sunlight.
2. Do not apply on injuries parts, malignant tumor and other abnormal parts.
3. This product is only for external use and not for internal use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HES CLEAN ADAM 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42979-120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	5.4 mg  in 180 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Menthol (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42979-120-01	180 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2014

Labeler - DOCTOR C&C (557816136)

Registrant - DOCTOR C&C (557816136)

Establishment
Name	Address	ID/FEI	Business Operations
DOCTOR C&C		557816136	manufacture(42979-120)