DR.PHI ADVANCED HAND SANITIZER gel

Dr.Phi Advanced Hand sanitizer by

Drug Labeling and Warnings

Dr.Phi Advanced Hand sanitizer by is a Otc medication manufactured, distributed, or labeled by MAMIBA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

ethyl alcohol % 70 V/V

purpose

antimicrobial 

uses

hand sanitizer to help reduce bacteria on the skin that could cause disease

INDICATIONS & USAGE

hand sanitizer to help reduce bacteria on the skin that could cause disease

warning

flamable , keep away from fire or flame

for external use only

keep out of reach of children

if swallowed get medical help or contact a poison control centre right away

when using this product

do not use in or near the eyes , in case of contact rinse eyes thoroughly with water

stop use and ask a doctor if

irritation and rash appears and lasts

directions

place enough prduct on your palm to thoroughly cover your hands

rub hands together until dry

other information

store below 110​°​ ​​F

may discolor certian fabrics or surfaces

inactive ingredients

water , glycerin , carbomer , PEG-40 hydrogentated castor oil , aminomethyl propanol, fragrance , EDTA disodium, BHT, tocopheryl acetate , aloe barbadensis (aloe vera) leaf extract.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.PHI ADVANCED HAND SANITIZER 
dr.phi advanced hand sanitizer gel

Product 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: 58161-156-08	40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2016
2	NDC: 58161-156-09	45 mL in 1 BOTTLE, PLASTIC; 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)