Label: HAND FOOT- cream cream
- NDC Code(s): 83872-310-01
- Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 13, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Ask Doctor
- Directions
- Other information
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Inactive ingredients
Water,Camellia Sinensis Leaf Extract,Cocos Nucifera(Coconut) Oil,Dodecane, Cetearyl Alcohol, Polysorbate 60,GlycerylStearate,PEG-100 Stearate,Cetyl Alcohol,Aloe Barbadensis LeafJuice,Melaleuca Alternifolia (Tea Tree)Leaf Oil,Glycerin,DipropyleneGlycol, Carbomer,Xanthan Gum, Ethylhexylglycerin,Caprylyl Glycol,Butyrospermum Parkii (Shea) Oil,Hexylene Glycol.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND FOOT
cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-310 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2.5 g in 50 mL 1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA (UNII: 0214C2T14J) (1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA - UNII:0214C2T14J) 1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA 5 g in 50 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) COCOS NUCIFERA WHOLE (UNII: 245J88W96L) POLYSORBATE 60 (UNII: CAL22UVI4M) PEG-100 STEARATE (UNII: YD01N1999R) CETYL ALCOHOL (UNII: 936JST6JCN) DIPROPYLENEGLYCOL DIGLYCIDYL ETHER (UNII: N7X2LEJ2HU) XANTHAN GUM (UNII: TTV12P4NEE) DODECANE (UNII: 11A386X1QH) MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU) WATER (UNII: 059QF0KO0R) CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-310-01 50 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product 07/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/13/2024 Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen Xiaomai Manufacturing Co., Ltd. 712999147 manufacture(83872-310)