MK STING RELIEF PADS- benzocaine, isopropyl alcohol liquid

MK Sting Relief Pads by

Drug Labeling and Warnings

MK Sting Relief Pads by is a Otc medication manufactured, distributed, or labeled by Changzhou Maokang Medical Products Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MK Sting Relief Pads

Active ingredients

Benzocaine 6.0%

Isopropyl Alcohol 60%

Purpose

Topical Analgesic

First Aid Antiseptic

Uses

• First aid to help prevent infection in minor cuts, scrapes, and burns
• First aid for the temporary relief of pain and itching in minor cuts, scrapes, and burns

Warnings

For external use only. Flammable, keep away from fire or flame.

Do not use

• in the eyes or apply over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if

• condition persists or gets worse
• 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

• Clean the affected area.
• Discard wipe after use.
• May be covered with a sterile bandage.
• If Bandaged, let dry first.
• Adults and children 2 years 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

Inactive ingredients:

Purified Water

MK Sting Relief Pads (

59050-414-20)

INGREDIENTS AND APPEARANCE

MK STING RELIEF PADS 
benzocaine, isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59050-414
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 mg  in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	60 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: 59050-414-20	200 in 1 BOX	06/09/2014
1		0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/09/2014

Labeler - Changzhou Maokang Medical Products Co., Ltd (421317073)

Establishment
Name	Address	ID/FEI	Business Operations
Changzhou Maokang Medical Products Co., Ltd		421317073	manufacture(59050-414)