PUROMA HAND SANITIZER- alcohol liquid

PUROMA Hand sanitizer by

Drug Labeling and Warnings

PUROMA Hand sanitizer by is a Otc medication manufactured, distributed, or labeled by ZENITH MICRO CONTROL. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol  75% V/V

Purpose

Antiseptic.

Warnings

• Flammable. Keep away from fire or flame.
• When using this product do not use in or near theeyes. In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears and lasts.

Uses

Hand Sanitizer to help reduce bacteria on skin.

Directions

• Spray enough product on hands to cover all surfaces. Rub hands together briskly until dry.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Other information

• Store below 110°F (43°C).
• May discolor certain fabrics or surfaces.

Inactive Ingredients

WATER, ISOPROPYL ALCOHOL ,GLYCERIN, ISOPROPYL MYRISTATE,ALPHA.-TOCOPHEROL ACETATE, CAPRYLYL GLYCOL, ALOE VERA LEAF, PROPYLENE GLYCOL,COCO-CAPRYLATE , FRAGRANCE.

Product Label

INGREDIENTS AND APPEARANCE

PUROMA HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80948-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCO-CAPRYLATE (UNII: 4828G836N6)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80948-003-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
2	NDC: 80948-003-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
3	NDC: 80948-003-03	50 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	12/20/2020
4	NDC: 80948-003-04	100 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	12/20/2020
5	NDC: 80948-003-05	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
6	NDC: 80948-003-06	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
7	NDC: 80948-003-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
8	NDC: 80948-003-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/20/2020
9	NDC: 80948-003-09	5000 mL in 1 CAN; Type 0: Not a Combination Product	12/20/2020
10	NDC: 80948-003-10	12 in 1 PACKAGE	10/19/2021
10		50 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
11	NDC: 80948-003-11	6 in 1 PACKAGE	10/19/2021
11		100 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/20/2020

Labeler - ZENITH MICRO CONTROL (915625571)