ECO BANDAGE SAND OCEAN- benzethonium chloride kit

Eco Bandage sand ocean by

Drug Labeling and Warnings

Eco Bandage sand ocean by is a Otc medication manufactured, distributed, or labeled by Eco Bandage LLC, Nitro Quimica Corporation dba Alchemix A Nitro Quimica Corporation, HK Kolmar Canada, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient                                        Purpose

Benzethonium chloride 0.2%....................... First aid antiseptic and skin protectant

PURPOSE

Uses

First aid to help prevent bacterial contamination and conceal minor cuts, scrapes and burns.
Hiding minor cuts and scrapes
Protect or prevent hangnails, blisters, and calluses.

Warnings

For external use only.

Flammable keep away from fire of flame

Do Not Use

On open or bleeding wounds.

In eyes or on mucus membranes.
Over large areas of body
On infected areas or bleeding or draining wounds
Deep cuts or puncture wounds
Animal bites
Serious burns
Longer than 1 week unless directed by healthcare professional
With other first aid products such as liquids, creams or lotions

Ask Doctor

Before use ask a healthcare professional if you have any of the following:

Serious bleeding
Diabetes
Poor circulation

When Using

Do not store at temperatures above 120 degrees F

Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal
Stop use and ask a healthcare professional if
Condition persists or gets worse
Infection occurs
Keep out of reach of children.
If swallowed, get medical help or call a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Direction

Clean and dry affected area.

Shake bottle well before use.
Wipe excess off brush
Apply a thin layer to a closed wound.
Let dry for 30 to 45 seconds.
Additional layers may be added once the previous layer has dried.

Other information

Eco Bandage wears off naturally.
To remove: simply peel off, apply coconut/olive oil or apply more Eco Bandage and quickly wipe off.
Store at room temperature (68-77°F, 20-25°C), away from heat.
Cap bottle tightly.
The antiseptic may temporarily sting upon application if the wound is open.

Inactive ingredients

amyl acetate, butyl acetate, USP castor oil, ethyl acetate, hypophosphorous acid, isopropanol, nitrocellulose, pigments, SD alcohol 3-C, SAIB.

Product label

INGREDIENTS AND APPEARANCE

ECO BANDAGE SAND OCEAN 
benzethonium chloride kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83829-006

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83829-006-01	1 in 1 KIT; Type 0: Not a Combination Product	03/05/2026

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	10 mL
Part 2	1 BOTTLE	10 mL

Part 1 of 2

ECO BANDAGE OCEAN 
benzethonium chloride liquid

Product Information
Item Code (Source)	NDC: 83829-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACETATE (UNII: 464P5N1905)
ETHYL ACETATE (UNII: 76845O8NMZ)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
AMYL ACETATE (UNII: 92Q24NH7AS)
ALCOHOL (UNII: 3K9958V90M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CASTOR OIL (UNII: D5340Y2I9G)
SUCROSE ACETATE ISOBUTYRATE (UNII: H5KI1C3YTV)
HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ)
PYROXYLIN (UNII: KYR8BR2X6O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83829-007-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003

Part 2 of 2

ECO BANDAGE SAND 
benzethonium chloride liquid

Product Information
Item Code (Source)	NDC: 83829-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACETATE (UNII: 464P5N1905)
ETHYL ACETATE (UNII: 76845O8NMZ)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
AMYL ACETATE (UNII: 92Q24NH7AS)
ALCOHOL (UNII: 3K9958V90M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CASTOR OIL (UNII: D5340Y2I9G)
SUCROSE ACETATE ISOBUTYRATE (UNII: H5KI1C3YTV)
HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ)
PYROXYLIN (UNII: KYR8BR2X6O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83829-008-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/05/2026

Labeler - Eco Bandage LLC (124618827)

Registrant - Eco Bandage LLC (124618827)

Establishment
Name	Address	ID/FEI	Business Operations
Nitro Quimica Corporation dba Alchemix A Nitro Quimica Corporation		615263956	manufacture(83829-006, 83829-007, 83829-008)

Establishment
Name	Address	ID/FEI	Business Operations
HK Kolmar Canada, Inc		243501959	manufacture(83829-006, 83829-007, 83829-008) , pack(83829-006, 83829-007, 83829-008)