GOLDSHIELD 24 GS 24- benzalkonium chloride solution

Pays: États-Unis

Langue: anglais

Source: NLM (National Library of Medicine)

Ingrédients actifs:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Disponible depuis:

AP GOLDSHIELD LLC

Mode d'administration:

TOPICAL

Type d'ordonnance:

OTC DRUG

indications thérapeutiques:

- Antiseptic/Antimicrobial - For hand washing to help reduce bacteria on the skin that could cause disease.

Statut de autorisation:

OTC monograph not final

Résumé des caractéristiques du produit

GOLDSHIELD 24 GS 24- BENZALKONIUM CHLORIDE SOLUTION
AP GOLDSHIELD LLC
_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._
----------
DRUG FACTS
GOLDSHIELD 24 ALCOHOL FREE ANTIBACTERIAL HAND FOAM RINSE contains 0.1
%
benzalkonium chloride antimicrobial agent, formulated with purified
water, propylene
glycol, methyl anthranilate and trihydroxysilylpropyldimethyloctadecyl
ammonium
chloride. Helps kill 99.99 % of germs and many common bacteria.
Moisturizes and
softens hands.
Benzalkonium Chloride 0.1 % ------------------------------------
Antimicrobial
Antiseptic/Antimicrobial
For hand washing to help reduce bacteria on the skin that could cause
disease.
Caution: For External Use Only. Avoid contact with eyes. In case of
contact flush
with water. Discontinue use if irritation or redness develops. If
condition persists for
more than 72 hours contact a physician.
Keep out of the Reach of Children. In case of accidental ingestion,
get medical help or
contact the Poison Control Center immediately.
Directions: Foam onto palm, massage into hands and fingernails and air
dry. Children
use with supervision.
Store at room temperature not below 32 degrees F.
Purified Water, Propylene Glycol, Methyl Anthranilate and
Trihydroxysilylpropyldimethyloctadecyl Ammonium Chloride
LABE
GOLDSHIELD 24 GS 24
benzalkonium chloride solution
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:40092-500
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
0.001 g
in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII:
IQ36O85WQ4)
METHYL ANTHRANILATE (UNII: 981I0C1E5W)
PRODUCT CHARACTERISTICS
COLOR