PHARMACYS PRESCRIPTION ALCOHOL WIPES- alcohol swab

Pharmacys Prescription Alcohol Wipes by

Drug Labeling and Warnings

Pharmacys Prescription Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by American Consumer Products Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredients - Ethyl Alcohol 75%

Purpose

Disinfectant

Uses

Helps reduce bacteria on the skin that could cause disease.

Warnings

Warnings - For external use only.

Flammable - Keep away from fire or flame.

Do not apply around eyes or use in ears & mouth.

When using this product

When using this product, avoid contact with eyes.

In case of contact flush eyes with water.

Stop use and ask a doctor

Strop use and ask doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children

Keep out of reach of children. Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions - Remove alcohol wipe from package. Thouroughly wipe skin, hands, fingers and wrists. Allow to dry. Discard after single use. Dispose of alcohol wipes in trash receptacle. Do not flush.

Other Information

Other information - this is not a baby wipe - store at 20°C (68° to 77°F).

- may discolor fabrics

INACTIVE INGREDIENTS

INACTIVE INGREDIENTS:

Water (Aqua), Aloe Essence Extract, Vitamin E, Phenoxyethanol, Sodium PCA, Benzalkonium Chloride, Sodium Carboxymethl Laurl Glucoside, Ethyl Glycerin, Cocamine DEA, Citric Acid

Distributed by

DISTRIBUTED BY:

American Consumer Products Corp.

VERNON, CA 90058

Made in China

Pharmacys Prescription Alcohol Wipes

INGREDIENTS AND APPEARANCE

PHARMACYS PRESCRIPTION ALCOHOL WIPES 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72197-029
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYL GLYCERIN ACETAL LEVULINATE (UNII: 7233JH4G65)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72197-029-10	10 mL in 1 BAG; Type 0: Not a Combination Product	05/21/2020
2	NDC: 72197-029-50	50 mL in 1 BAG; Type 0: Not a Combination Product	05/21/2020
3	NDC: 72197-029-80	80 mL in 1 BAG; Type 0: Not a Combination Product	05/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/21/2020

Labeler - American Consumer Products Corp (081101181)