FDA.reportPublic FDA data

Dr.Phi Advanced Hand sanitizer

Manufacturer
MAMIBA
Effective date
2020-05-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:57

Label at a glance#

ProductDr.Phi Advanced Hand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

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

Dosage and administration

place enough prduct on your palm to thoroughly cover your hands rub hands together until dry

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol % 70 V/V

purpose

OTC - PURPOSE SECTION

antimicrobial 

uses

DOSAGE & ADMINISTRATION SECTION

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

INDICATIONS & USAGE SECTION

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

warning

WARNINGS SECTION

flamable , keep away from fire or flame

for external use only

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

when using this product

OTC - WHEN USING SECTION

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

stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and rash appears and lasts

directions

INSTRUCTIONS FOR USE SECTION

place enough prduct on your palm to thoroughly cover your hands

rub hands together until dry

other information

OTHER SAFETY INFORMATION

store below 110​°​ ​​F

may discolor certian fabrics or surfaces

inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 ml10 ml

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136224007379004GTIN-13: 6224007379004
EAN-13: 6224007379004
GTIN storage (14 digits): 06224007379004		Dr.phi tube 10 ml.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58161-15658161-156-14, 58161-156-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
POLYOXYL 40 CASTOR OIL4ERD2076EFIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAF POLYSACCHARIDESW21O437517IACT
FD&C BLUE NO. 1H3R47K3TBDCNTM
FD&C YELLOW NO. 5I753WB2F1MCNTM
EXT. D&C VIOLET NO. 2G5UX3K0728CNTM
FD&C RED NO. 4X3W0AM1JLXCNTM
FD&C YELLOW NO. 6H77VEI93A8CNTM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d21a970a-dc7e-400b-b3ee-ceb3fd50951373486bbd-7fb8-443e-a29c-81f4006febd12021-08-09WarningsExact identifier
spl set id: 73486bbd-7fb8-443e-a29c-81f4006febd1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.