TEMPO BZK TOWELETTE- benzalkonium chloride cloth TEMPO ALCOHOL PREP PAD- isopropyl alcohol swab TEMPO STING RELIEF PAD- benzocaine, isopropyl alcohol swab

Tempo Sting Relief Pad by

Drug Labeling and Warnings

Tempo Sting Relief Pad by is a Otc medication manufactured, distributed, or labeled by Tempo Medical Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Product Label for NDC:

71756-8050-1 (BZK Towelette)

Directions

Tear open pouch, unfold and use. Discard after single use.

Warnings

• For external use only
• Flammable, keep away from open flame

Inactive Ingredient

purified water, camphor

Do Not Use / Stop Use / Use

(Do not use)

• On irritated skin or over large areas of the body
• If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

Cleansing of hands, face and body. Air dries in seconds.

Keep out of reach of children

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

Purpose

Antiseptic Cleanser

Active Ingredient

Benzalkonium Chloride 0.13% v/v

Product Label for NDC:

71756-8010-1 (Alcohol Prep Pad)

Directions

Wipe injection site and discard after single use.

Warnings

• For external use only
• Flammable, keep away from open flame

Inactive Ingredient

purified water

Do Not Use / Stop Use / Use

(Do not use)

• With electrocautery procedures
• If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

For preparation of the skin prior to an injection

Keep out of reach of children

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

Purpose

Antiseptic

Active Ingredient

Isopropyl Alcohol 70% v/v

Product Label for NDC:

71756-8090-1 (Sting Relief Pad)

Directions

Clean intended area with pad and discard after single use.

Warnings

• For external use only
• Flammable, keep away from open flame

Inactive Ingredient

purified water

Do Not Use / Stop Use / Use

(Do not use)

• With electrocautery procedures
• If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Keep out of reach of children

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

Purpose

Topical Anesthetic (Benzocaine)

Antiseptic (Isopropyl Alcohol)

Active Ingredient

Benzocaine 6% v/v

Isopropyl Alcohol 70% v/v

INGREDIENTS AND APPEARANCE

TEMPO BZK TOWELETTE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71756-8050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71756-8050-1	1.5 mg in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	12/27/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/27/2012

TEMPO ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71756-8010
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: 71756-8010-1	0.45 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	03/08/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/08/2010

TEMPO STING RELIEF PAD 
benzocaine, isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71756-8090
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
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 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: 71756-8090-1	0.45 mg in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	09/30/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/30/2016

Labeler - Tempo Medical Products (786585963)