ADHESIVE REMOVER WIPES- isopropyl alcohol cloth

Adhesive Remover Wipes by

Drug Labeling and Warnings

Adhesive Remover Wipes by is a Otc medication manufactured, distributed, or labeled by Ningbo Riway Daily Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Isopropyl Alcohol 1%v/v

Purpose

Antiseptic

Use

For the removal of adhesive residue on skin.

Warnings

For external use only.Flammable.Keep away from fire or flame.

Do not use

If you are allergic to any of the ingredients.

WHEN USING

When using this product,avoid contact with eyes and mouth. If product gets in the eyes,flush thoroughly with water.

STOP USE

Discontinue use and contact a doctor if irritation and redness develop and condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Tear open packet and remove wipe.

Wipe the skin thoroughly.

Throw used wipe in trash. Do not flush.

Inactive ingredients

Aloe Barbadensis Extract,Ethylhexylglycerin,Iodopropynyl Butylcarbamate,Isododecane,Phenoxyethanol,Purified water,Tocopheryl Acetate

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ADHESIVE REMOVER WIPES 
isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77267-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	1 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ISODODECANE (UNII: A8289P68Y2)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77267-006-01	60 in 1 BOX	10/17/2020	03/31/2024
1		4 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 77267-006-02	50 in 1 BOX	03/28/2024
2		4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/17/2020

Labeler - Ningbo Riway Industrial Co., Ltd. (540997562)

Registrant - Ningbo Riway Industrial Co., Ltd. (540997562)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Riway Industrial Co., Ltd.		540997562	manufacture(77267-006)