SALINE WOUND WASH SIGNATURE CARE- benzethonium chloride liquid

Saline Wound Wash by

Drug Labeling and Warnings

Saline Wound Wash by is a Otc medication manufactured, distributed, or labeled by Better Living, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                                             Purpose
Benzethonium Chloride 0.13%.........................................................Topical anesthetic

PURPOSE

Uses

First aid to help prevent the rick of bacterial contamination in minor cuts, scrapes and burns

WARNINGS

Warnings
For external use only.

Do not use in the eyes longer than 1 week
When using this product  avoid spraying in eyes

Do not puncture or incenerate. Contents under pressure. Do not store at temperature above 120F
Stop use and ask a doctor if condition worsens or persists

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Directions

• clean the affected area
• spray a small amount of this product on the area 1 to 3 times a day
• may be covered with steriline bandage
• if bandage, let dry first

Inactive ingredients

BENZALKONIUM CHLORIDE

ALOE VERA LEAF

water

SODIUM BICARBONATE

SODIUM CHLORIDE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SALINE WOUND WASH  SIGNATURE CARE
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21130-762
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzethonium Chloride (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	Benzethonium Chloride	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
water (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21130-762-05	201 g in 1 CAN; Type 1: Convenience Kit of Co-Package	03/30/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2018

Labeler - Better Living (009137209)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(21130-762) , label(21130-762)