Label: HWASAMONG DR.ALL SCALP HEALINGSHAMPOO- betaine, panthenol shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 76678-0001-1 - Packager: Eolracellbio Co., Ltd.
- 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 May 2, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Water
Disodium Cocoamphodiacetate
Sodium Cocoyl Isethionate
Potassium Cocoyl Glycinate
Lauryl Glucoside
Decyl Glucoside
Glycerin
LoniceraJaponica(Honeysuckle)FlowerExtract
EcliptaProstrataExtract
CitrusUnshiuPeelExtract
MenthaArvensisExtract
PolygonumMultiflorumRootExtract
BiotaOrientalisLeafExtract
MorusAlbaLeafExtract
HouttuyniaCordataExtract
GlycineSoja(Soybean)SeedExtract
EckloniaCavaExtract
PerillaFrutescensLeafExtract
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Arginine
Polyquaternium-10
Allantoin
Niacinamide
Butylene Glycol
1,2-Hexanediol
Caprylyl Glycol
Illicium Verum (Anise) Fruit Extract
Citric Acid
Disodium EDTA
Sodium Hyaluronate
Zinc Pyrithione
Menthol
Fragrance - INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HWASAMONG DR.ALL SCALP HEALINGSHAMPOO
betaine, panthenol shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76678-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETAINE (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W) BETAINE 0.5 g in 100 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength NIACINAMIDE (UNII: 25X51I8RD4) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76678-0001-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/03/2020 Labeler - Eolracellbio Co., Ltd. (694875102) Registrant - Eolracellbio Co., Ltd. (694875102) Establishment Name Address ID/FEI Business Operations Eolracellbio Co., Ltd. 694875102 manufacture(76678-0001)