Label: POWERBOOSTER ORIGINAL- witch hazel, caffeine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70843-001-01, 70843-001-02 - Packager: Peterpanlab
- 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 July 26, 2018
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Isopropyl Palmitate, Butylene Glycol, Cetyl Ethylhexanoate, Stearic Acid, Hydrogenated Polydecene, Cetearyl Alcohol, Glyceryl Stearate, Glycerin, Polysorbate 60, Butyrospermum Parkii (Shea) Butter, Dimethicone, Vanillyl Butyl Ether, Ethyl Hexanediol, PEG-100 Stearate, Beeswax, Sorbitan Sesquioleate, Tocopheryl Acetate, Carbomer, Tromethamine, Glyceryl Caprylate, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, , Squalane, Fragrance, Xanthan Gum, Disodium EDTA, Glycolic Acid, 1,2-Hexanediol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POWERBOOSTER ORIGINAL
witch hazel, caffeine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70843-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 0.098 g in 100 mL CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 0.01 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) STEARIC ACID (UNII: 4ELV7Z65AP) HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 60 (UNII: CAL22UVI4M) SHEA BUTTER (UNII: K49155WL9Y) DIMETHICONE (UNII: 92RU3N3Y1O) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) ETHOHEXADIOL (UNII: M9JGK7U88V) PEG-100 STEARATE (UNII: YD01N1999R) YELLOW WAX (UNII: 2ZA36H0S2V) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) TROMETHAMINE (UNII: 023C2WHX2V) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) SQUALANE (UNII: GW89575KF9) XANTHAN GUM (UNII: TTV12P4NEE) GLYCOLIC ACID (UNII: 0WT12SX38S) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70843-001-02 1 in 1 CARTON 07/26/2018 1 NDC:70843-001-01 100 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/26/2018 Labeler - Peterpanlab (689040427) Registrant - Peterpanlab (689040427) Establishment Name Address ID/FEI Business Operations ATEC Co., Ltd. 689276681 manufacture(70843-001)