CVS BURN RELIEF W/LIDO 8OZ- lidocaine hcl gel

CVS Burn Relief w/Lido 8oz by

Drug Labeling and Warnings

CVS Burn Relief w/Lido 8oz by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Lidocaine HCl 0.5%

Purpose

Topical Analgesic

Uses

• Temporarily relieves pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, or minor skin irritations.
  

Warnings

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. If contact occurs, rinse thoroughly with water.
  

Stop use and ask a doctor if

• irritation or rash develops
• 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 swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 years and older:apply to affected areas as needed, not more than 3 to 4 times a day
• children under 2 years:ask a doctor before use
  

Inactive ingredients

Water, Propylene Glycol, Glycerin, Isopropyl Alcohol, Triethanolamine, Polysorbate 80, Carbomer, Aloe Barbadensis Leaf Juice Powder, Menthol, Disodium EDTA, Diazolidinyl Urea, Yellow 5, Blue 1.

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Compare to Solarcaine

Burn Relief Gel

NEW!

BURN RELIEF GEL

WITH LIDOCAINE HCl

RESTORES MOISTURE

• Soothes and relieves

• Cooling sunburn relief

• Topical analgesic gel

NET WT 8 OZ (226 g)

INGREDIENTS AND APPEARANCE

CVS BURN RELIEF W/LIDO 8OZ 
lidocaine hcl gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-670
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-670-16	226 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/08/2015

Labeler - CVS Pharmacy (062312574)