- Active Ingredient
- Purpose
- Uses
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Warnings
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- For external use only: Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns, consult a physician.
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- Allergy Alert: Do not use if you are allergic to any of the ingredients in this product.
- Directions
- Other information
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Inactive ingredients
alcohol, aloe barbadensis leaf juice, arginine, butylparaben, cetearyl isononanoate, dipropylene glycol dicaprylate/dicaprate, ethylparaben, eucalyptus globulus leaf oil, hexyl decyl laurate, hexyldecanole, melaleuca alternifolia (tea tree) leaf oil, menthol, methylparaben, ozokerite, phenoxyethanol, poloxamer 407, propylparaben, thymol, tocopheryl nicotinate (vitamin e), zinc chloride
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INGREDIENTS AND APPEARANCE
UP AND UP COLD SORE TREATMENT
camphor creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-407 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 30 mg in 1 g BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARGININE (UNII: 94ZLA3W45F) BUTYLPARABEN (UNII: 3QPI1U3FV8) CERESIN (UNII: Q1LS2UJO3A) CETEARYL ISONONANOATE (UNII: P5O01U99NI) PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA) ETHYLPARABEN (UNII: 14255EXE39) HEXYLDECANOL (UNII: 151Z7P1317) CETYL LAURATE (UNII: I19DN3Q5ZP) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) METHYLPARABEN (UNII: A2I8C7HI9T) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLOXAMER 407 (UNII: TUF2IVW3M2) PROPYLPARABEN (UNII: Z8IX2SC1OH) TEA TREE OIL (UNII: VIF565UC2G) TOCOPHERYL NICOTINATE, D-.ALPHA. (UNII: WI1J5UCY5C) THYMOL (UNII: 3J50XA376E) ZINC CHLORIDE (UNII: 86Q357L16B) EUCALYPTOL (UNII: RV6J6604TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-407-01 1 in 1 PACKAGE 04/05/2013 1 2 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/05/2013 Labeler - Target Corporation (006961700)