FRANKLIN CLEANING TECHNOLOGY ANTIBACTERIAL HAND- chloroxylenol liquid

Franklin cleaning technology antibacterial hand by

Drug Labeling and Warnings

Franklin cleaning technology antibacterial hand by is a Otc medication manufactured, distributed, or labeled by Fuller Industries, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Chloroxylenol 0.3%

Purpose

Antiseptic

Uses

• For hand washing to decrease the bacteria on skin.
• Recommended for repeated use

Warnings

For external use only

Do not use

in the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• Pump a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together to produce a thick lather
• Rinse and repeat

Inactive ingredients

DEIONIZED WATER, SODIUM LAURYL ETHER SULFATE, SODIUM CHLORIDE, COCAMIDE MIPA, SODIUM SULFATE, OCEAN BREEZE FRAGRANCE 16295, MAGNESIUM NITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD & C YELLOW #6, D&C RED NO. 33

Package Labeling:

INGREDIENTS AND APPEARANCE

FRANKLIN CLEANING TECHNOLOGY ANTIBACTERIAL HAND 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60933-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
SODIUM SULFATE (UNII: 0YPR65R21J)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60933-056-00	3790 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/28/2023

Labeler - Fuller Industries, Inc (078704329)

Establishment
Name	Address	ID/FEI	Business Operations
Fuller Industries, Inc		078704329	manufacture(60933-056)