Hand Sanitizer Liquids

To help reduce bacteria, fungi, and viruses on the skin.

Isopropyl Alcohol 70% v/v - Antimicrobial

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Place a small amount of product in your palm to thoroughly cover your hands.
Rub hands together briskly until dry.
Children under 6 years should be supervised when using this product.

Aloe Vera, Dragon's Breath Essential Oil Blend (Essential oils of Clove, Lemon, Cinnamon Bark, Eucalyptus, Peppermint, Oregano), Hydrogen Peroxide, Sodium Citrate

Place a small amount of product in your palm

For external use only.
Flammable.
Keep away from fire or flame.
Do not use in eyes. In case of eye contact, flush thoroughly with water.
Discontinue use if irritation or redness develops.
If condition persists for more than 72 hours, consult a doctor.

Chupps 2oz 003-02 8 oz spray label euc mint spray dragon 60 spray sf spray 1oz Full label upload Lemon Eucalyptus Mint 8oz

DB 4 oz DB 16oz

Lavender 8oz

Lemon 8oz

Antiseptic Spray

Antiseptic Spray Lemon 2 ounce Spray

antiseptic spray 0 Lavender 2 oz spray

4 oz label

HAND SANITIZER LIQUID WITH LAVENDER
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-004
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)
LAVENDER OIL (UNII: ZBP1YXW0H8)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73769-004-30	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020
2	NDC:73769-004-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/10/2020
3	NDC:73769-004-60	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/16/2020

HAND SANITIZER LIQUID WITH LEMON
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-005
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)
LEMON OIL (UNII: I9GRO824LL)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73769-005-30	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020
2	NDC:73769-005-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/10/2020
3	NDC:73769-005-60	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/16/2020

NATURES FUSIONS DRAGONS BREATH HAND SANITIZER LIQUID
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-001
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
CLOVE OIL (UNII: 578389D6D0)
EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
OREGANO LEAF OIL (UNII: 7D0CGR40U1)
PEPPERMINT OIL (UNII: AV092KU4JH)
CINNAMON BARK OIL (UNII: XE54U569EC)
LEMON OIL (UNII: I9GRO824LL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73769-001-30	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	03/16/2020
2	NDC:73769-001-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020
3	NDC:73769-001-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020
4	NDC:73769-001-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/27/2020
5	NDC:73769-001-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/29/2020
6	NDC:73769-001-01	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/27/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/16/2020

UNSCENTED HAND SANITIZER LIQUID
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-000
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73769-000-30	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/16/2020

MINT/EUCALYPTUS/LEMON HAND SANITIZER LIQUID
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-002
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
EUCALYPTUS OIL (UNII: 2R04ONI662)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
LEMON OIL (UNII: I9GRO824LL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73769-002-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020
2	NDC:73769-002-08	236.6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/27/2020
3	NDC:73769-002-04	113 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/16/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/16/2020

HAND SANITIZER LIQUID WITH IMMUNITY
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-003
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
CLOVE OIL (UNII: 578389D6D0)
EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CINNAMON BARK OIL (UNII: XE54U569EC)
LEMON OIL (UNII: I9GRO824LL)
SODIUM PERCARBONATE (UNII: Z7G82NV92P)
ROSEMARY OIL (UNII: 8LGU7VM393)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73769-003-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/13/2020

ANTIBAC ON THE GO
isopropanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73769-006
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
THYME OIL (UNII: 2UK410MY6B)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
LEMON OIL (UNII: I9GRO824LL)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73769-006-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/26/2020
2	NDC:73769-006-04	118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/26/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	08/26/2020

Labeler - NATURE'S FUSIONS, LLC (051472644)

Name	Address	ID/FEI	Business Operations
Establishment
NATURE'S FUSIONS, LLC		051472644	manufacture(73769-000, 73769-001, 73769-002, 73769-003, 73769-004, 73769-005, 73769-006)