Label: YOULIEF NIGHT HIBIPAIRCREAM- adenosine, ginger root extract, hibiscus syriacus bark extract cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73560-0001-1 - Packager: Plcoskin
- 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 27, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
water, glycerin, butylene glycol dicaprylate/dicaprate, hydrogenated polyisobutene, dipentaerythrityl hexa C5-9 acid esters, glycereth-26, coco-caprylate/caprate, butyrospermum parkii(shea) butter, glyceryl stearate, cetearyl alcohol, polyglyceryl-3 distearate, 1,2-hexanediol, polyglyceryl-3-methylglucose distearate, ammonium acryloyldimethyltaurate/VP copolymer, dimethicone, sodium stearoyl glutamate, hydroxyethyl acrylate/sodium acryloyldimethhyl taurate copolymer, sodium polyacrylate, C12-16 alcohols, squalane, ethylhexylglycerin, glyceryl stearate citrate, fructooligosaccharides, saccharide hydrolysate, hydrogenated lecithin, palmitic acid, polysorbate-60, pullulan, disodium EDTA, butylene glycol, sodium hyaluronate, bifida ferment lysate, sorbitan isostearate, hyaluronic acid, potassium sorbate, citric acid, titanium dioxide
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
For external use only
When using this product■ if the following symptoms occurs after use, stop use and consult with a skin specialist
red specks, swelling, itching
■ don’t use on the part where there is injury, eczema, or dermatitis
Keep out of reach of children
■ if swallowed, get medical help or contact a person control center immediately
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YOULIEF NIGHT HIBIPAIRCREAM
adenosine, ginger root extract, hibiscus syriacus bark extract creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73560-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HIBISCUS SYRIACUS BARK (UNII: U6PQI719P3) (HIBISCUS SYRIACUS BARK - UNII:U6PQI719P3) HIBISCUS SYRIACUS BARK 0.002 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 0.0001 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73560-0001-1 60 mL in 1 TUBE; Type 0: Not a Combination Product 01/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/22/2020 Labeler - Plcoskin (694845185) Registrant - Plcoskin (694845185) Establishment Name Address ID/FEI Business Operations Shinsegae Intercos Korea Inc. 694526100 manufacture(73560-0001) Establishment Name Address ID/FEI Business Operations Plcoskin 694845185 label(73560-0001)
