FDA.reportPublic FDA data

Dr.Phi Antibacterial hand wash

Manufacturer
MAMIBA
Effective date
2020-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:23

Label at a glance#

ProductDr.Phi Antibacterial hand wash
Active ingredientTRICLOSAN
Label structure12 sections

Indications and uses

HELP TO REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE

Dosage and administration

APPLY 1.5 ml OF THE PRODUCT ON WET HANDS, WORK INTO LATHER, RINSE WELL AND DRY HANDS COMPLETELY.

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

Triclosan 0.3%

purpose

OTC - PURPOSE SECTION

ANTIBACTERIAL

uses

DOSAGE & ADMINISTRATION SECTION

HELP TO REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE

INDICATIONS & USAGE SECTION

HELP TO REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE

warning

WARNINGS SECTION

FOR EXTERNAL USE ONLY

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

when using this product

OTC - WHEN USING SECTION

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.

stop use and ask a doctor if

OTC - STOP USE SECTION

IRRITATION OR RASH DEVELOPS AND LASTS

DIRECTIONS FOR USE

INSTRUCTIONS FOR USE SECTION

APPLY 1.5 ml OF THE PRODUCT ON WET HANDS, WORK INTO LATHER, RINSE WELL AND DRY HANDS COMPLETELY.

other information

OTHER SAFETY INFORMATION

store below 30°C

inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, SODIUM LAURETH SULFATE, COCAMIDE DEA, POLYQUATERNIUM-10, FRAGRANCE, CITRIC ACID, SODIUM CHLORIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.
MAY CONTAIN: CI61570, CI15985, CI16255, CI14720, CI16185.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58161-16058161-160-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRICLOSAN4NM5039Y5XACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
D&C GREEN NO. 58J6RDU8L9XCNTM
FD&C YELLOW NO. 6H77VEI93A8CNTM
PONCEAU 4RZ525CBK9PGCNTM
FD&C BLUE NO. 1H3R47K3TBDCNTM
FD&C YELLOW NO. 5I753WB2F1MCNTM

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
bf2826fa-2690-4eb5-a8b3-1de4b5679dba1f1c4bc3-61cd-4630-9d76-c717ecdd387e2021-08-04WarningsExact identifier
spl set id: 1f1c4bc3-61cd-4630-9d76-c717ecdd387e

Reported adverse events (FAERS/openFDA)#

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