CVS BLISTER RELIEF REFILL PACK- benzalkonium chloride kit

CVS Blister Relief Refill Pack by

Drug Labeling and Warnings

CVS Blister Relief Refill Pack by is a Otc medication manufactured, distributed, or labeled by CVS, Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride .13%

Purpose

First Aid Antiseptic

Use

For Professional and Hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.

Warnings

For external use only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If unusual redness, swelling or other symptoms occur, cunsult a physician immediately.

KEEP OUT OF REACH OF CHILDREN

STOP USE

Do not use

In the eyes, or over large areas of the body

Directions

Tear open packet, unfold towelette and use to cleanse desired skin are. Discard towelette appropriately after single use

Inactive Ingredients

Purified Water

Antiseptic Towelette

Antiseptic Towelette
GFA Production Xiamen Co., Ltd
www.gfaproduction.com

INGREDIENTS AND APPEARANCE

CVS BLISTER RELIEF REFILL PACK 
benzalkonium chloride kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-406

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-406-00	1 in 1 BAG; Type 0: Not a Combination Product	12/01/2016

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	8 PACKAGE	6 mL  in .8

Part 1 of 1

ANTISEPTIC 
benzalkonium chloride swab

Product Information
Item Code (Source)	NDC: 52124-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0001-1	0.8 mL in 1 PACKAGE; 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	part333E	12/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333A	12/01/2016

Labeler - CVS (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(69842-406)