Available Formats

• Active ingredient

  Dimethicone 1.75%

  Purpose

  Skin Protectant
  

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• Uses

  â–  temporarily protects and helps relieve chapped or cracked skin

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• Warnings

  For external use only

  Do not use on

  â–  deep or puncture wounds    â–  animal bites    â–  serious burns

  When using this product

  â–  do not get into eyes

  Stop use and ask a doctor if

  â–  condition worsens
  â–  symptoms last more than 7 days or clear up and occur again within a few days

  Keep out of reach of children.

  If swallowed, get medical help or contact a Poison Control Center right away.

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• Directions

  â–  apply cream liberally as needed

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• Other information

  â–  protect from freezing    â–  avoid excessive heat

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• Inactive ingredients

  Aleurites moluccana seed oil, Aloe barbadensis (Aloe vera) leaf juice, butylene glycol, Carthamus tinctorius (safflower) seed oil, cetyl alcohol, dimethicone crosspolymer, disodium EDTA, fragrance, glycerin, glyceryl stearate, GenRx Complexâ„¢ [consisting of: bisabolol, calcium pantothenate (vitamin B5), Carthamus tinctorius (safflower) oleosomes, maltodextrin, niacinamide (vitamin B3), pyridoxine HCl (vitamin B6), silica, sodium ascorbyl phosphate (vitamin C), sodium starch octenylsuccinate, tocopheryl acetate (vitamin E), Zingiber officinale (ginger) root extract], PEG-100 stearate, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, purified water, sodium hyaluronate, stearic acid, triethanolamine.

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• Daily Defense Skin Repairing Cream with GenRx Complex​TM (4 fl. oz tube label)

  

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• INGREDIENTS AND APPEARANCE

  GENRX DAILY DEFENSE SKIN REPAIRING  dimethicone cream

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-829 Route of Administration TOPICAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O) Dimethicone 17.5 mg  in 1 mL

  Inactive Ingredients Ingredient Name Strength KUKUI NUT OIL (UNII: TP11QR7B8R)   ALOE VERA LEAF (UNII: ZY81Z83H0X)   BUTYLENE GLYCOL (UNII: 3XUS85K0RA)   SAFFLOWER OIL (UNII: 65UEH262IS)   CETYL ALCOHOL (UNII: 936JST6JCN)   DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)   EDETATE DISODIUM (UNII: 7FLD91C86K)   GLYCERIN (UNII: PDC6A3C0OX)   GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)   LEVOMENOL (UNII: 24WE03BX2T)   CALCIUM PANTOTHENATE (UNII: 568ET80C3D)   CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)   MALTODEXTRIN (UNII: 7CVR7L4A2D)   NIACINAMIDE (UNII: 25X51I8RD4)   PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)   SILICON DIOXIDE (UNII: ETJ7Z6XBU4)   SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)   .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)   GINGER (UNII: C5529G5JPQ)   PEG-100 STEARATE (UNII: YD01N1999R)   PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)   PHENOXYETHANOL (UNII: HIE492ZZ3T)   WATER (UNII: 059QF0KO0R)   HYALURONATE SODIUM (UNII: YSE9PPT4TH)   STEARIC ACID (UNII: 4ELV7Z65AP)   TROLAMINE (UNII: 9O3K93S3TK)

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-829-69 144 in 1 CARTON 1 NDC:59088-829-01 4 mL in 1 POUCH 2 NDC:59088-829-05 59 mL in 1 TUBE 3 NDC:59088-829-08 118 mL in 1 TUBE

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/08/2013

  Labeler - PureTek Corporation (785961046)

  Establishment
  Name	Address	ID/FEI	Business Operations
  PureTek Corporation		785961046	manufacture(59088-829) , pack(59088-829) , label(59088-829)

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