PURMIST- chlorhexidine gluconate, ethyl alcohol solution

Purmist by

Drug Labeling and Warnings

Purmist by is a Otc medication manufactured, distributed, or labeled by MKR International Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Kills 99.99% of germs while moisturizing hands

WHEN USING

WHEN TO USE: PURMIST® is suggested to be applied after any contact with other people or objects. PURMIST® is safe to use before or after meals for adults or children.

DIRECTIONS: Remove cap. Spray as needed in hand and rub hands together covering all areas, including the fingernail areas thoroughly. Replace cap securely after use or discard. Dries in seconds. Childproof bottle.

ACTIVE INGREDIENT

ACTIVE INGREDIENTS: Ethyl Alcohol 70% w/w, Chlorhexidine Gluconate 1% w/w

OTHER INGREDIENTS: A blend of Natural Essential Oils, Polysorbate 20, Water

DO NOT USE

WARNING: Flammable. Keep away from fire or flames. Do not spray in eyes. Avoid spraying directly on face or near face. First Aid: If sprayed in eyes, hold eyes open and flush thoroughly with water for 15 minutes. Consult a physician immediately if irritation continues.

CAUTION: FOR EXTERNAL USE ONLY

• Use by children under the age of 5 should be under an adult's supervision due to possible unknown allergic reactions.
• Discontinue use if irritation occurs on hands.
• If pregnant or allergic, consult a physician before use.
• Not to be taken internally.
  

PURMIST® 7.1mL / 0.24 fl. oz

NDC: 50353-103-10

PURMIST® 0.24 fl. oz

Hand Sanitizer
KILLS 99.99% OF GERMS
Made with natural essential oils
Kills harmful bacteria and germs while moisturizing hands
ENERGIZING ORANGE

PURMIST® 100mL / 3.38 fl. oz

PURMIST®

Hand Sanitizer
KILLS 99.99% OF GERMS
ONLY EFFECTIVE PRODUCT TO
NATURALLY PROVIDE
4 hour
PROTECTION
with each application!

ENERGIZING ORANGE
Made with Natural Essential Oils

NDC: 50353-103-50
3.38 fl.oz.

INGREDIENTS AND APPEARANCE

PURMIST 
chlorhexidine gluconate, ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50353-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	.7 g  in 1 mL
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50353-103-10	1 in 1 BLISTER PACK
1		7.1 mL in 1 BOTTLE, PUMP
2	NDC: 50353-103-50	6 in 1 CARTON
2		100 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	06/01/2010

Labeler - MKR International Inc (243605685)