CARESOUR ALCOHOL WIPES cloth

Caresour Alcohol Wipes by

Drug Labeling and Warnings

Caresour Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Imperial Palace Commodity(Shenzhen)CO.,LTD, Imperial Palace Commodity(Dongguan)CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 75%

PURPOSE

Cleaning and disinfection

INDICATIONS & USAGE

Uses

Packs

Peel back lid and then label.
Remove wipes as required.
Replace lid and label to keep wipes moist.

Buckets

Open the bucket lid from the top.
Locate tear cut in the inner pouch, tear straight to open. Do not remove wipesroll from pouch.
Pull first wipes from center of roll up through opening.
Thread first wipe through dispensing nozzle in top of roll.
Close the bucket lid and dispense the wipes as required.

WARNINGS

For external use only.
Store in cool and dry place.keep away from heat and direct sunlight.
Avoid touching eyes. In case of eye contact, flush thoroughly with water.
Avoid contact with broken skin.
Don't flush into toilet.
Stop use and ask a doctor if skin irritation develops.

In case of accidental ingestion, seekprofessional assistance or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Thoroughly moisten the skin or solid surface with the product and let it dry without wiping
For children under 6, use only under adult supervision.
Not recommended for infants.

INACTIVE INGREDIENT

Water, Glycerin

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CARESOUR ALCOHOL WIPES 
caresour alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52489-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	591 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52489-004-01	350 mL in 1 BAG; Type 0: Not a Combination Product	09/26/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/26/2024

Labeler - Imperial Palace Commodity(Shenzhen)CO.,LTD (527796368)

Registrant - Imperial Palace Commodity(Dongguan)CO.,LTD (544367643)

Establishment
Name	Address	ID/FEI	Business Operations
Imperial Palace Commodity(Dongguan)CO.,LTD		544367643	manufacture(52489-004)