ADVENTURE FIRST AID .5 TIN- benzocaine, alcohol, benzalkonium chloride kit

Adventure First Aid .5 Tin by

Drug Labeling and Warnings

Adventure First Aid .5 Tin by is a Otc medication manufactured, distributed, or labeled by Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient - Antiseptic

Benzalkonium Chloride 0.13%

Purpose - Antiseptic

Antiseptic

Use - Antiseptic

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

Warnings, Precautions and Directions - Antiseptic

For External use only.

Keep out of Reach of Children.

Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.

Do not uses in eyes or over large areas of the body.

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

Inactive Ingredients - Antiseptic

Purified Water

Active Ingredient - Alcohol Prep Pad

Isopropyl Alcohol 70%

Use - Alcohol Prep Pad

For preparation of the skin before injection

Warnings, Precautions and Directions - Alcohol Prep Pad

For External Use Only

Flammable - Keep away from fire or flame

Do Not Use - with electrocautery, in eyes

Stop Use and Ask a Doctor if - Irritation or redness develop and 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.

Tear Open packet, unfold and use as and wipe injection site vigorously and discard.

Store at Room Temperature

Active Ingredients - Insect Relief Pad

Benzocaine 6%

SD alcohol 60%

Purpose - Insect Relief Pad

Topical Anesthetic - Antiseptic

Use - Insect Relief Pad

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

Warnings, Precautions and Directions - Insect Relief Pad

Clean intended area thoroughly with pad. Discard after single use

Warnings: For external use only.

Avoid contact with eyes. If this happens, rinse thoroughly with water

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

Flammable - keep away from fire or flame

Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

Active Ingredients - Triple Antibiotic Ointment

Bacitracin Zinc 400 units

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

Polymyxin B Sulfate 5000 units

Purpose - Triple Antibiotic Ointment

Triple Antibiotic

Use - Triple Antibiotic Ointment

To help prevent infection in: minor cuts; scrapes and burns

Warnings, Precautions and Directions - Triple Antibiotic Ointment

For external use only.

Do not use: in eyes; over large areas of the body;

If allergic to any of the ingredients; for more than one week unless directed by a physician

Stop use and consult a doctor: if the condition persists or gets worse; a rash or other allergic reaction develops.

Keep out of reach of children.

If ingested, contact a Poison Control Center right away

Directions: clean affected area; apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage.

Adventure First Aid .5 Tin

INGREDIENTS AND APPEARANCE

ADVENTURE FIRST AID .5 TIN 
benzocaine, alcohol, benzalkonium chloride kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-0203

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-0203-1	1 in 1 BOX; Type 0: Not a Combination Product	10/01/2015

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	2 PACKAGE	1 mL  in .5
Part 2	4 PACKAGE	3 mL  in .7
Part 3	4 PACKAGE	3 mL  in .8
Part 4	4 TUBE	2 g  in .5

Part 1 of 4

INSECT STING RELIEF PAD 
benzocaine,alcohol swab

Product Information
Item Code (Source)	NDC: 52124-0008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	0.6 mg  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 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: 52124-0008-1	0.5 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	part348	04/23/2011

Part 2 of 4

ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC: 52124-0017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	700 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: 52124-0017-1	0.7 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	part333A	02/01/2016

Part 3 of 4

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	part333A	04/23/2010

Part 4 of 4

GENUINE TRIPLE ANTIBIOTIC 
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment

Product Information
Item Code (Source)	NDC: 52124-0003
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0003-1	0.5 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	12/28/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2015

Labeler - Tender Corporation (064437304)

Registrant - Tender Corporation (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(44224-0203)