SOPURO ANTIBACTERIAL HAND CLEANER FRAGRANCE FREE- alcohol gel

Sopuro by

Drug Labeling and Warnings

Sopuro by is a Otc medication manufactured, distributed, or labeled by Previcare Pharmaceutical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethanol (Ethyl Alcohol) 70% V/V

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable.

Do not ingest. Keep away from heat or flame.

Do not use

• If you are allergic to any ingredient.
• On open wounds.

When using this product

Avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation develops.

Keep out of reach of children. If swallowed, get medical help.

Directions

• Apply to one palm, rub hands together until dry.
• Use as part of your daily cleaning routine.
• Do not rinse with water, do not dilute the product.
• Supervise children when using this product.

Other information

Store at 15-30°C (59-86°F).

Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

Aqua, glycerin, aloe barbadensis (Aloe) leaf juice, PEG-75 lanolin, myristyl alcohol, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, PEG-7 glyceryl cocoate.

SPL UNCLASSIFIED SECTION

Distributed by: Previcare Pharmaceutical, Inc.
50 Fountain Plaza, Suite 1400
Buffalo, NY 14202

PRINCIPAL DISPLAY PANEL - 500 ml Bottle Label

Antibacterial Hand Cleaner

Fragrance Free

sopuro

16.9 fl. oz
500 ml

Aloe Vera Enriched
Moisturizing Gel

70 %
Ethyl Alcohol

INGREDIENTS AND APPEARANCE

SOPURO   ANTIBACTERIAL HAND CLEANER FRAGRANCE FREE
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73401-975
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 VERA LEAF (UNII: ZY81Z83H0X)
PEG-75 LANOLIN (UNII: 09179OX7TB)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73401-975-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2020
2	NDC: 73401-975-02	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2020
3	NDC: 73401-975-09	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	11/01/2020

Labeler - Previcare Pharmaceutical, Inc. (117180835)