APLICARE PHYSICIANS ANTIBACTERIAL- triclosan liquid

Aplicare Physicians Antibacterial by

Drug Labeling and Warnings

Aplicare Physicians Antibacterial by is a Otc medication manufactured, distributed, or labeled by Aplicare Products, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Triclosan

Purpose

Antiseptic

Use

antibacterial skin cleanser

Warnings

For external use only

Avoid contact with the eyes

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Directions

• add small amount of APLICARE Physician's Antibacterial Soap to wet hands and forearms
  
• develop lather
• scrub well and rinse thoroughly after washing
  

Other information

• Reduces bacteria that can potentially cause disease
  

Inactive ingredients

acrylates/steareth-20 methacrylate copolymer, citric acid, DMDM hydantoin, FDandC yellow no. 5, fragrance, lauramide DEA, polyquaternium-7, propylene glycol, sodium C12-15 pareth-15 sulfonate, sodium hydroxide, sodium lauryl sulfate, tetrasodium EDTA, water

PRINCIPAL DISPLAY PANEL

Aplicare

Physician's Antibacterial Soap

INGREDIENTS AND APPEARANCE

APLICARE PHYSICIANS ANTIBACTERIAL 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52380-1845
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
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
DMDM HYDANTOIN (UNII: BYR0546TOW)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
LAURAMIDE (UNII: 3BD22052MO)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52380-1845-4	130 g in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	07/01/2020
2	NDC: 52380-1845-9	3955 g in 1 BOTTLE; Type 0: Not a Combination Product	02/20/2018	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/1998	07/01/2020

Labeler - Aplicare Products, LLC. (081054904)

Establishment
Name	Address	ID/FEI	Business Operations
Aplicare Products, LLC.		081054904	manufacture(52380-1845)