PHARMACYS PRESCRIPTION ALCOHOL WIPES- alcohol swab 
American Consumer Products Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Pharmacys Prescription Wipes

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

Pharmacys Prescription 10 Count WipesPharmacys Prescription 50 Count WipesPharmacys Prescription 80 Count Wipes

PHARMACYS PRESCRIPTION ALCOHOL WIPES 
alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-029
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72197-029-1010 mL in 1 BAG; Type 0: Not a Combination Product05/21/2020
2NDC:72197-029-5050 mL in 1 BAG; Type 0: Not a Combination Product05/21/2020
3NDC:72197-029-8080 mL in 1 BAG; Type 0: Not a Combination Product05/21/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/21/2020
Labeler - American Consumer Products Corp (081101181)

Revised: 6/2020
Document Id: a79d1db0-782c-0189-e053-2a95a90a0660
Set id: a62f4f24-6e03-a499-e053-2a95a90a2040
Version: 2
Effective Time: 20200608
 
American Consumer Products Corp