- active ingredient
- purpose
- uses
- INDICATIONS & USAGE
- warning
- keep out of reach of children
- when using this product
- stop use and ask a doctor if
- directions
- other information
- inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.PHI ADVANCED HAND SANITIZER
dr.phi advanced hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58161-156 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER 940 (UNII: 4Q93RCW27E) POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517) Other Ingredients Ingredient Kind Ingredient Name Quantity May contain FD&C BLUE NO. 1 (UNII: H3R47K3TBD) May contain FD&C YELLOW NO. 5 (UNII: I753WB2F1M) May contain EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) May contain FD&C RED NO. 4 (UNII: X3W0AM1JLX) May contain FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58161-156-01 10 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2016 Labeler - MAMIBA (558528988) Establishment Name Address ID/FEI Business Operations MAMIBA 558528988 manufacture(58161-156)