GENUINE FIRST AID PAIN RELIEVING CREAM- benzalkonium chloride, lidocaine hydrochloride cream

Pajjiż: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ingredjent attiv:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y), LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)

Disponibbli minn:

GFA Production (Xiamen) Co., Ltd.

Rotta amministrattiva:

TOPICAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

- Temporary relief of pain associated with minor cuts, scrapes, and burns. - Helps pretect against harmful bacteria.

Karatteristiċi tal-prodott

GENUINE FIRST AID PAIN RELIEVING CREAM- BENZALKONIUM CHLORIDE,
LIDOCAINE
HYDROCHLORIDE CREAM
GFA PRODUCTION (XIAMEN) CO., LTD.
----------
GENUINE FIRST AID PAIN RELIEVING CREAM
DRUG FACTS
_ACTIVE INGREDIENTS_
Benzalkonium Chloride 0.13%
Lidocaine HCl 0.5%
_PURPOSE_
First Aid Antiseptic
Topical Analgesic
_USES_
Temporary relief of pain associated with minor cuts, scrapes, and
burns.
Helps pretect against harmful bacteria.
_WARNINGS_
FOR EXTERNAL USE ONLY.
DO NOT USE
• in eyes • in large quantities • over raw or blistered areas,
or on deep puncture
wounds, animal bites, or serious burns • for more than one week
unless directed by a
doctor
KEEP OUT OF THE REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
directly.
_DIRECTIONS_
clean affected area
apply small amount not more than 3 times daily
may be covered with a sterile bandage
_OTHER INFORMATION_
store in a cool dry area 15° to 25° C (59° to 79°F)
tamper evident sealed packets
do not use any opened or torn packets
_INACTIVE INGREDIENTS_
Aloe Barbadensis Leaf Juice, Cetearyl Alcohol, Disodium EDTA,
Ethylhexylglycerin,
Glycerin, Glyceryl Stearate/PEG-100 Stearate, Maltodextrin, Mineral
Oil, Phenoxyethanol,
Propylene Glycol, Purified Water, Stearic Acid, Triethanolamine
PACKAGE LABELING:
GENUINE FIRST AID PAIN RELIEVING CREAM
benzalkonium chloride, lidocaine hydrochloride cream
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:50814-079
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6JUD5X6Y)
BENZ ALKONIUM
CHLORIDE
1.3 mg
in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE -
UNII:98PI200987)
LIDOCAINE
5 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE/PEG-100 STE