ALCOHOL WIPES cloth

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Available from:

Wenzhou Guanshang Paper Co., Ltd

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antiseptic. Do not use in eyes, wounds and other sensitive parts. Stop use if irritation and redness develop. If condition continues, consult your health care practitioner. Apply to the sterilization and cleaning for hand, skin and daily supplies.

Authorization status:

OTC monograph not final

Summary of Product characteristics

ALCOHOL WIPES- ALCOHOL WIPES CLOTH
WENZHOU GUANSHANG PAPER CO., LTD
_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._
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78122-103 GUANSHANG, 75% ALCOHOL WIPES, PAIL
ACTIVE INGREDIENT
Alcohol 75% v/v. Purpose: Antiseptic
PURPOS E
Antiseptic.
WHEN USING
Avoid using in eyes, wounds and other sensitive parts.
If it gets into eyes accidentally, please wash it with plenty of
water.
DO NOT USE
Do not use in eyes, wounds and other sensitive parts.
STOP USE
Stop use if irritation and redness develop. If condition continues,
consult your health care practitioner.
KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children.
INDICATIONS & USAGE
Apply to the sterilization and cleaning for hand, skin and daily
supplies.
DIRECTIONS
1. Unscrew the end, Open the inner packing bag
2. Pull out the Wet wipe, put it through A small hole in the end
3. Tighten the lid and open it Small cover on top, wet extraction
Towel to self breaking place
4. After use, the Cover tightly again to ensure Keep wet
WARNINGS
For external use only.
Flammable, please stay away from fire!
OTHER INFORMATION
Store away from directly sunlight.
INACTIVE INGREDIENT
Water.
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
ALCOHOL WIPES
alcohol wipes cloth
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:78 122-10 3
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
2.6 25 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:78 122-10 3-17
6 0 in 1 PAIL; Type 0 : No t a Co mbinatio n Pro duct
0 6 /0 2/20 20
2
NDC:78 122-10 3-21
8 0 in 1 PAIL; Type 0 : No t a Co mbinatio n Pro duct
0 6 /0 2/20 20
3
NDC:78 122-10 3-25
10 0 in 1 PAIL; Type 0 :