GERMISEPT ANTIBACTERIAL ALCOHOL WIPES- alcohol cloth

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

Jurong Dongfa General Merchandise Co., Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

- For cleansing to decrease bacteria on skin. - Recommended for repeated use with a new unused wipe each time. - Dries quickly.

Authorization status:

OTC monograph not final

Summary of Product characteristics

GERMISEPT ANTIBACTERIAL ALCOHOL WIPES- ALCOHOL CLOTH
JURONG DONGFA GENERAL MERCHANDISE 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._
----------
75127-008 GERMISEPT ANTIBACTERIAL ALCOHOL WIPES
DRUGS FACT
ACTIVE INGREDIENT
Ethyl Alcohol 75%(v/v)
PURPOSE
Antiseptic
USES:
For cleansing to decrease bacteria on skin.
Recommended for repeated use with a new unused wipe each time.
Dries quickly.
WARNINGS
FLAMMABLE,KEEP AWAY FROM FIRE OR FLAME.
FOR EXTERNAL USE ONLY.
DO NOT USE
in or contact the eyes.
Discontinue use if irritation and redness develop. If condition
persists for more than
72 hours, consult a physician.
KEEP THIS OUT OF REACH OF CHILDREN.
unless under adult supervision.
If swallowed, get medical help or contact a Poison Control Center
immediately.
DIRECTIONS
Open the flip top lid, remove one wipe to use.
Wipe hands thoroughly with product and allow to dry without wiping.
Close filp top lid label after use to retain moisture.
OTHER INFORMATION
Dispose of wipe in the proper container.
Do not flush down the toilet.
INACTIVE INGREDIENTS
Aloe Barbadensis Leaf Extract, Aqua (Purified & De-Ionized Water),
Benzalkonium
Chloride, Glycerin.
PACKAGE LABELING:
GERMISEPT ANTIBACTERIAL ALCOHOL WIPES
alcohol cloth
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:75127-008
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
0.75 mL in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
GLYCERIN (UNII: PDC6A3C0OX)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:75127-
008-01
24 in 1 CARTON
10/20/2020
1
50 in 1 BAG
1
305 g in 1 NOT APPLICABLE; Type 0: Not a
Combination Product
2
NDC