DR.PHI ANTIBACTERIAL HAND WASH liquid

Dr.Phi Antibacterial hand wash by

Drug Labeling and Warnings

Dr.Phi Antibacterial hand wash by is a Otc medication manufactured, distributed, or labeled by MAMIBA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

Triclosan 0.3%

purpose

ANTIBACTERIAL

uses

HELP TO REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE

INDICATIONS & USAGE

HELP TO REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE

warning

FOR EXTERNAL USE ONLY

keep out of reach of children

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

when using this product

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

stop use and ask a doctor if

IRRITATION OR RASH DEVELOPS AND LASTS

DIRECTIONS FOR USE

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

other information

store below 30°C

inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.PHI ANTIBACTERIAL HAND WASH 
dr.phi antibacterial hand wash liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58161-162
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
May contain	FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
May contain	PONCEAU 4R (UNII: Z525CBK9PG)
May contain	FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
May contain	FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58161-162-02	10 in 1 CARTON	03/01/2020
1	NDC: 58161-162-01	500 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2020

Labeler - MAMIBA (558528988)

Establishment
Name	Address	ID/FEI	Business Operations
MAMIBA		558528988	manufacture(58161-162)