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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dr.Phi advanced hand sanitizer

active ingredient

ethyl alcohol % 70 V/V

purpose

antimicrobial 

uses

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

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.

2ml

DR.PHI ADVANCED HAND SANITIZER 
dr.phi advanced hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58161-156
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 KindIngredient NameQuantity
May containFD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
May containFD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
May containEXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
May containFD&C RED NO. 4 (UNII: X3W0AM1JLX)  
May containFD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58161-156-208 in 1 CARTON04/01/202005/01/2020
1200 in 1 CARTON
1NDC:58161-156-192 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/202005/01/2020
Labeler - MAMIBA (558528988)
Establishment
NameAddressID/FEIBusiness Operations
MAMIBA558528988manufacture(58161-156)

Revised: 9/2021
Document Id: c20696a7-759e-4416-94dc-4a84e7636162
Set id: cff574e3-03ae-440f-a15a-5a8ae5013177
Version: 12
Effective Time: 20210923
 
MAMIBA