Label: CLAON ALL 4 CLEANSER- lauryl glucoside liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70694-0002-1 - Packager: Inc MBG
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated January 24, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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INDICATIONS & USAGE
Hair
After soaking hair with warm water, pour a moderate amount onto the hands, gently massage the product onto the scalp and hair, and then wash out the product thoroughly.
Shaving
With warm water, wet the area that will be shaved, pour a moderate amount and create a foam, shave, and then wash out the product thoroughly.
Body
Take a moderate amount of product and put onto a shower puff or sponge, massage the entire body, and then wash out the product thoroughly.
Foam Cleanser
Wet the entire face, pour a moderate amount and create a foam, gently massage the face and then wash out the product thoroughly with warm water - KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- WARNINGS
- PURPOSE
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INACTIVE INGREDIENT
Purified Water (Medi-Hocl), Potassium Olivoyl/Lauroyl Wheat Amino Acids, TEA-Cocoyl Glutamate, Disodium Cocoamphodiacetate, Babassuamidopropyl Betaine, Glycerin, PEG-120 Methyl Glucose Dioleate, Niacinamide, Zanthoxylum Piperitum Fruit Extract, Pulsatilla Koreana Extract, Usnea Barbata (Lichen) Extract, Flavoring, Polyquaternium-10 , Panthenol, Black Soybean Extract, Hydrolyzed Keratin, Salicylic Acid, Disodium EDTA
- ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLAON ALL 4 CLEANSER
lauryl glucoside liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70694-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) (LAURYL GLUCOSIDE - UNII:76LN7P7UCU) LAURYL GLUCOSIDE 16.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70694-0002-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/24/2019 Labeler - Inc MBG (688436167) Establishment Name Address ID/FEI Business Operations Inc MBG 688436167 manufacture(70694-0002)