W/CLIP PDQ INSTANT HAND SANITIZER- ethyl alcohol kit

W/CLIP PDQ INSTANT HAND SANITIZER by

Drug Labeling and Warnings

W/CLIP PDQ INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INSTANT HAND SANITIZER Citrus Zest

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

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

Directions

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients

aqua(water), acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, aloe barbadensis leaf juice, CI 14700, CI 19140, denatonium benzoate, fragrance, glycerine, propylene glycol, tocopheryl acetate

INSTANT HAND SANITIZER Lavender

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

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

Directions

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients

aqua(water), acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, aloe barbadensis leaf juice, CI 17200, CI 42090, denatonium benzoate, fragrance, glycerine, propylene glycol, tocopheryl acetate

INSTANT HAND SANITIZER Aloe Vera

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

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

Directions

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients

aqua(water), acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, aloe barbadensis leaf juice, CI 19140, CI 42090, denatonium benzoate, fragrance, glycerine, propylene glycol, tocopheryl acetate

INSTANT HAND SANITIZER Classic

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

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

Directions

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients

aqua(water), acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, aloe barbadensis leaf juice, denatonium benzoate, fragrance, glycerine, propylene glycol, tocopheryl acetate

SPL UNCLASSIFIED SECTION

With Vitamin E & Other Moisturizers

KILLS GERMS WITHOUT RINSE

Convenient Size

Moisturizes with Vitamin E

ASSORTED

Made in China

Mfd for and Distributed by:
UNIVERSAL DISTRIBUTION CENTER LLC
330 Applegarth Road,
Monroe Township, NJ 08831
www.universaldc.com

Packaging

INGREDIENTS AND APPEARANCE

W/CLIP PDQ INSTANT HAND SANITIZER 
ethyl alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-423

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-423-24	1 in 1 BOX; Type 0: Not a Combination Product	04/09/2025

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	6 BOTTLE	328.2 mL
Part 2	6 BOTTLE	328.2 mL
Part 3	6 BOTTLE	328.2 mL
Part 4	6 BOTTLE	328.2 mL

Part 1 of 4

INSTANT HAND SANITIZER CITRUS ZEST 
ethyl alcohol gel

Product Information
Item Code (Source)	NDC: 52000-424
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)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-424-24	54.7 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	505G(a)(3)	04/09/2025

Part 2 of 4

INSTANT HAND SANITIZER LAVENDER 
ethyl alcohol gel

Product Information
Item Code (Source)	NDC: 52000-425
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)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-425-24	54.7 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	505G(a)(3)	04/09/2025

Part 3 of 4

INSTANT HAND SANITIZER ALOE VERA 
ethyl alcohol gel

Product Information
Item Code (Source)	NDC: 52000-426
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)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-426-24	54.7 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	505G(a)(3)	04/09/2025

Part 4 of 4

INSTANT HAND SANITIZER CLASSIC 
ethyl alcohol gel

Product Information
Item Code (Source)	NDC: 52000-427
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)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-427-24	54.7 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	505G(a)(3)	04/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/09/2025

Labeler - Universal Distribution Center LLC (019180459)