Label: HWASAMONG DR.ALL SCALP HEALING TONIC (lonicerajaponica- honeysuckleflowerextract liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76678-0002-1 - 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 10, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
EcliptaProstrataExtract
CitrusUnshiuPeelExtract
MenthaArvensisExtract
PolygonumMultiflorumRootExtract
BiotaOrientalisLeafExtract
MorusAlbaLeafExtract
GlycineSoja(Soybean)SeedExtract
EckloniaCavaExtract
PerillaFrutescensLeafExtract
Camellia Sinensis Leaf Extract
Perilla Frutescens Leaf Extract
llicium Verum (Anise) Fruit Extract
Butylene Glycol
Caprylyl Glycol
1.2-Hexanediol - INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HWASAMONG DR.ALL SCALP HEALING TONIC
lonicerajaponica(honeysuckle)flowerextract liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76678-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) (LONICERA JAPONICA FLOWER - UNII:4465L2WS4Y) LONICERA JAPONICA FLOWER 10 g in 100 mL HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T) (HOUTTUYNIA CORDATA WHOLE - UNII:O3E12ZLW5T) HOUTTUYNIA CORDATA WHOLE 7 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76678-0002-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2020 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(76678-0002)