Global Household Antibacterial Wild Berry Fresh Scent

Global Household Antibacterial Wild Berry Fresh Scent by

Drug Labeling and Warnings

Global Household Antibacterial Wild Berry Fresh Scent by is a Otc medication manufactured, distributed, or labeled by TARGET PRICE, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GLOBAL HOUSEHOLD ANTIBACTERIAL WILD BERRY FRESH SCENT- chloroxylenol liquid 
TARGET PRICE, INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Global Household Antibacterial Wild Berry Fresh Scent

Drug Facts

Active ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Keep Out of reach of children.

In case of accidental ingestion, drink a glass of water to dilute. if eye contact occurs, rinse thoroughly with water.

Directions.

Wet hands and forearms. Apply 5 ml or palmfu to hands and forearms. Scrub thoroughly for 30 seconds and rinse.

Inactive ingredients.

water, sodium, lauril sulfate, lauramine oxide, sodium laureth sulfate, alcoholdenat., phenoxyethanol, sodium chloride, PPG-26, PEI-14 PGE24/PPG-16 copolymer, sodium hydroxide, fragrance, C9-11, pareth-8, tetrasodium glumate diacetate, yellow 5, methylisothiazoinone, blue 1

Package Labeling:354.88ml

Package Labeling:739.33ml

GLOBAL HOUSEHOLD ANTIBACTERIAL WILD BERRY FRESH SCENT 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72146-041
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 (UNII: 9NEZ333N27)
LAURYL SULFATE (UNII: DIQ16UC154)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PPG-26 (UNII: V86KZL3H2Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
C9-11 PARETH-8 (UNII: 80E6PSE1XL)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72146-041-00	354.88 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020	11/18/2021
2	NDC: 72146-041-01	739.33 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020	11/18/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020	11/18/2021

Labeler - TARGET PRICE, INC. (081086884)

Revised: 11/2021

Document Id: d126d870-9612-bb75-e053-2995a90ad67d

34390-5

Set id: ae7fd341-d664-8e3d-e053-2a95a90ae92f

Version: 2

Effective Time: 20211119