GOOD SENSE BURN RELIEF ALOE- lidocaine hcl gel

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)

Available from:

Geiss, Destin & Dunn, Inc

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

External Analgesic. Adults and children 2 years and older: apply to the affected area, not more than 3 to 4 times a day. Children under 2 years of age: consult a physician.

Authorization status:

OTC monograph not final

Summary of Product characteristics

GOOD SENSE BURN RELIEF ALOE- LIDOCAINE HCL GEL
GEISS, DESTIN & DUNN, INC
_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._
----------
BURN RELIEF, LIDOCAINE HCL 0.5%
Lidocaine HCl 0.5%
External Analgesic.
For the temporary relief of pain and itching due to sunburn, minor
burns, insect bites,
minor cuts, scrapes, and minor skin irritations.
FOR EXTERNAL USE ONLY.
DO NOT USE in large quantities, particularly over raw surfaces or
blistered areas.
WHEN USING THIS PRODUCT avoid contact with eyes. Rinse with water if
contact occurs.
STOP USE AND ASK A DOCTOR if the condition worsens or symptoms persist
for more
than 7 days or clear up and occur again within a few days.
KEEP OUT OF REACH OF CHILDREN. If the product is swallowed, get
medical help or
contact a Poison Control Center right away.
Adults and children 2 years and older: apply to the affected area, not
more than 3 to 4
times a day. Children under 2 years of age: consult a physician.
Water, Glycerin, Isopropyl Alcohol, Aloe Barbadensis Leaf Extract,
Menthol, Propylene
Glycol, Polysorbate 80, Triethanolamine, Carbomer, Disodium EDTA, Blue
1, Yellow 5,
Diazolidinyl Urea.
GOOD SENSE BURN RELIEF ALOE
lidocaine hcl gel
PRODUCT INFORMATION
Geiss, Destin & Dunn, Inc
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:50804-955
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE -
UNII:98PI200987)
LIDOCAINE HYDROCHLORIDE
ANHYDROUS
0.5 g
in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MENTHOL (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 940 (UNII: 4Q93RCW27E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
DIAZ