CVS HEALTH HEALING ON THE GO KIT- isopropyl alcohol, bacitracin zinc,neomycin sulfate,polymyxin b sulfate, benzocaine kit

CVS Health Healing on the Go Kit by

Drug Labeling and Warnings

CVS Health Healing on the Go Kit by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy Inc, Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Use

For preparation of skin before injection.

Warnings

For external use only.

Flammable - keep away from fire or flame

Do not use

• in the eyes
• with electrocautery procedures

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

Wipe Injection site vigorously and discard.

Other Information

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

Inactive Ingredient

purified water

ACTIVE INGREDIENTS

Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

PURPOSE

First Aid Antibiotic

USE

First aid to help prevent infection in minor cuts, scrapes, and burns.

WARNINGS

For external use only.

DO NOT USE

• if you are allergic to any of the ingredients
• in the eyes
• over large areas of the body

Ask a doctor before use if you have

• deep pumcture wounds
• animal bites
• serious burns

STOP USE AND ASK A DOCTOR IF

Symptoms persist for more than 7 days or clear up and occur again within a few days.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• adults and children 2 year of age and older: clean the affected area; apply a small amount to the area 1-3 times daily; may be covered with a sterile bandage
• children under 2 years of age: consult a doctor

Inactive Ingredients

mineral oil, petrolatum

ACTIVE INGREDIENTS

Benzocaine, 6%

SD alcohol, 60%

PURPOSE

Topical Analgesic
Antiseptic

USE

temporarily relieves pain and itching due to minor stings and insect bites

WARNINGS

For external use only.

Flammable, keep away from fire or flame.

DO NOT USE

• over large areas of the body
• in the eyes
• on broken skin or deep puncture wounds

STOP USE AND ASK A DOCTOR IF

condition worsens or if symptoms persist for more than 7 days or clears up and occurs again within a few days.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

• adults and children 2 year of age and older: apply to affected area not more than 3 to 4 times daily.
• children under 2 years of age: consult a doctor

OTHER INFORMATION

Store at room temperature

INACTIVE INGREDIENT

Purified water

PRINCIPAL DISPLAY PANEL

Easy Care First Aid® Skin Cleansing Alcohol Wipe

Responsibly made in China for:

Tender Corporation

944 Industrial Park Rd.

Littleton, NH 03561
easycarefirstaid.com

1 single use wipe

PRINCIPAL DISPLAY PANEL

Easy Care First Aid

Triple Antibiotic Ointment

Responsibly Made in China for:

Tender Corporation

Littleton, NH 03561

easycarefirstaid.com

PRINCIPAL DISPLAY PANEL

After Bite Wipe Insect Sting Relief

1 single use wipes

Responsibly made in China for:

Tender Corporation

944 Industrial park Rd.

Littleton, NH

afterbite.com

INGREDIENTS AND APPEARANCE

CVS HEALTH HEALING ON THE GO KIT 
isopropyl alcohol, bacitracin zinc,neomycin sulfate,polymyxin b sulfate, benzocaine kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-418

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-418-01	1 in 1 KIT; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	09/01/2019

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	5 POUCH	2.5 mL
Part 2	2 TUBE	1.8 g
Part 3	1 PACKAGE	1000 mg

Part 1 of 3

EASY CARE FIRST AID SKIN CLEANSING ALCOHOL WIPE 
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC: 44224-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-0010-0	0.5 mL in 1 POUCH; 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	part333A	09/02/2019

Part 2 of 3

EASY CARE FIRST AID TRIPLE ANTIBIOTIC 
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment

Product Information
Item Code (Source)	NDC: 44224-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	400 [iU]  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-0013-4	0.9 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	09/01/2019

Part 3 of 3

AFTER BITE WIPE INSECT STING RELIEF 
benzocaine,alcohol swab

Product Information
Item Code (Source)	NDC: 44224-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 mg  in 100 mg
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mg  in 100 mg

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-0014-1	1000 mg 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	09/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2019

Labeler - CVS Pharmacy Inc (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(69842-418)