SANITIZING HAND MIST UNSCENTED- ethyl alcohol spray SANITIZING HAND MIST LEMONGRASS- ethyl alcohol spray SANITIZING HAND GEL UNSCENTED- ethyl alcohol gel SANITIZING HAND GEL PEPPERMINT EUCALYPTUS- ethyl alcohol gel SANITIZING HAND MIST PEPPERMINT EUCALYPTUS- ethyl alcohol spray SANITIZING HAND GEL LEMONGRASS- ethyl alcohol gel

Sanitizing Hand Gel Lemongrass by

Drug Labeling and Warnings

Sanitizing Hand Gel Lemongrass by is a Otc medication manufactured, distributed, or labeled by ALO New York LLC, Alkaline Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Ethyl Alcoahol

Purpose

Antiseptic

Uses

For handwashing to decrease bacteria on the skin

Warnings

Flammable. Keep away from fire or flame. For external use only.

When using this product

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask doctor if

irritation and redness develop and persist.

Keep out of reach of chidren.

If swallowed, get medical help promptly.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other information

Store under 105°F

Inactive Ingredients

NDC: 80588-010:
Water, Glycerine, Aloe Barbadensis Leaf
NDC: 80588-011:
Water, Glycerine, Alce Barbadensis Leaf, Eucalyptus Radiata Flower/leaf/Stem Oil, Piper Mentha Piperita (Peopermint) Oil

NDC: 80588-012:

Water, Glycerine, Aloe Barbadensis Leaf, Cymbopogon Schoenanthus (Lemongrass) Oil

NDC: 80588-020:
Water, Glyperine, Rapidgel EZ. Aloe barbadensis Leaf
NDC: 80588-011:
Water. Glycerine, Rapidgel EZ. Aloe Barbadensis Leaf. Eucalyptus Radiate Flower/Leaf/Stem Oil, Piper Mentha Piperita (Peppermint) Oil

NDC: 80588-012:
Water, Glycerine, Rapidgel EZ. Aloe Barbadensis Leaf, Cymbopogon Schoenanthus (Lemongrass) Oil

Sanitizing Hand Mist - Lemongrass +Aloe NDC:

82355-012-02

Sanitizing Hand Gel ReCharge - Peppermint Euclyptus +Aloe NDC:

82355-021-32

Sanitizing Hand Gel ReCharge Lemongrass + Aloe NDC:

82355-022-32

Sanitizing Hand Gel ReCharge - Unscented + Aloe NDC:

82355-020-32

Sanitizing Hand Mist - Peppermint Eucalyptus + Aloe NDC:

82355-011-02

Sanitizing Hand Mist - Unscented + Aloe NDC:

82355-010-02

Sanitizing Hand Mist - Lemongrass +Aloe NDC:

82355-012-08

Sanitizing Hand Mist - Peppermint Eucalypyus + Aloe NDC:

82355-011-08

Sanitizing Hand Mist - Unscented + Aloe NDC:

82355-010-08

Sanitizing Hand Gel - Lemongrass + Aloe NDC:

82355-022-08

Sanitizing Hand Gel - Peppermint Eucalyptus + Aloe NDC:

82355-021-08

Sanitizing Hand Gel - Unscented + Aloe NDC:

82355-020-08

INGREDIENTS AND APPEARANCE

SANITIZING HAND MIST UNSCENTED 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-010-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/09/2022
2	NDC: 82355-010-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/09/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/09/2022

SANITIZING HAND MIST LEMONGRASS 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-012-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/06/2022
2	NDC: 82355-012-08	238 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/06/2022

SANITIZING HAND GEL UNSCENTED 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-020-08	238 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/09/2022
2	NDC: 82355-020-32	900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/09/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/09/2022

SANITIZING HAND GEL PEPPERMINT EUCALYPTUS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EUCALYPTUS OIL (UNII: 2R04ONI662)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-021-08	238 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/06/2022
2	NDC: 82355-021-32	900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/06/2022

SANITIZING HAND MIST PEPPERMINT EUCALYPTUS 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
PEPPERMINT OIL (UNII: AV092KU4JH)
EUCALYPTUS OIL (UNII: 2R04ONI662)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-011-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/06/2022
2	NDC: 82355-011-08	238 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/06/2022

SANITIZING HAND GEL LEMONGRASS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-022-08	238 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/06/2022
2	NDC: 82355-022-32	900 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/06/2022

Labeler - ALO New York LLC (110122374)

Registrant - Alkaline Corporation (790098318)

Establishment
Name	Address	ID/FEI	Business Operations
Alkaline Corporation		790098318	manufacture(82355-010, 82355-011, 82355-012, 82355-020, 82355-021, 82355-022) , pack(82355-010, 82355-011, 82355-012, 82355-020, 82355-021, 82355-022) , label(82355-010, 82355-011, 82355-012, 82355-020, 82355-021, 82355-022)