CWGC (as PLD) - SIERRA SOFT SANITIZING WET WIPES 75% ETHYL ALCOHOL (70415-109) - DELIST

SANITIZING WET WIPES by

Drug Labeling and Warnings

SANITIZING WET WIPES by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc., Fujian Yifa Healthcare Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SANITIZING WET WIPES 75 PERCENT- ethyl alcohol solution 
CWGC LA Inc.

----------

CWGC (as PLD) - SIERRA SOFT SANITIZING WET WIPES 75% ETHYL ALCOHOL (70415-109) - DELIST

Active ingredient

Alcohol 75%

PURPOSE

ANTISEPTIC

Uses

FOR HAND WASHING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEAT USE.

Warnings

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

DO NOT USE IF YOU ARE ALLERGIC TO ANY OF THE INGREDIENTS.

DISCONTINUE USE IF IRRITATION OR REDNESS DEVELOPS, AND IF CONDITION PERSISTS FOR MORE THAN 72 HOURS CONSULT A PHYSICIAN.

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

KEEP OUT OF REACH OF CHILDREN UNLESS UNDER ADULT SUPERVISION.

IF SWALLOWED, GET MEDICAL HELP, OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Directions

OPEN RESEALABLE LABEL AND PULL ONE SHEET FROM PACK. THOROUGHLY CLEAN HANDS OR AFFECTED AREA AND DISCARD IN RECEPTACLE, AND DO NOT FLUSH. ALLOW TO DRY WITHOUT WIPING. BE SURE TO RESEAL LABEL COMPLETE TO RETAIN MOISTURE.

Inactive ingredients

WATER (AQUA), GLYCERINE, ALOE ESSENCE EXTRACT, VITAMIN E, PHENOXYETHANOL, BETAINE, BENZALKONIUM CHLORIDE.

SANITIZING WET WIPES  75 PERCENT
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70415-109
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BETAINE (UNII: 3SCV180C9W)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70415-109-50	50 in 1 POUCH	08/15/2020	12/31/2022
1		10 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/15/2020	12/31/2022

Labeler - CWGC LA Inc. (034967904)

Revised: 9/2023

Document Id: 05dfc63b-68d9-55fd-e063-6294a90aad84

34390-5

Set id: 1205e43e-18e8-49e2-9964-9b53eb081021

Version: 7

Effective Time: 20230921

 <