SELECT BRAND BURN RELIEF- lidocaine hcl gel

Select Brand Burn Relief by

Drug Labeling and Warnings

Select Brand Burn Relief by is a Otc medication manufactured, distributed, or labeled by Select Brand Distributors. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Lidocaine HCL 0.50%

Purpose

Topical Anesthetic

Uses

• temporary relief of pain and itching
  
• helps relieve and soothes pain from sunburn, minor burns,cuts,scrapes, skin irritations and insect bites

Warnings

For external use only

When using this product

• avoid contact with eyes.
• do not use in large quantities, particularly over raw surfaces or blistered areas
  

Stop use and ask a doctor if

• condition worsens or if symptoms persist for more than 7 days.
• if symptoms clear up and occur again within a few days.

Keep out of reach of children.
If swallowed get medical help or contact Poison Control Center immediately.

Directions

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
• children under 2 years of age: ask a doctor
  

Inactive ingredients

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

Principal Display Panel

select brand
the lower price name brand
BURN RELIEF
ALOE VERA GEL
with
LIDOCAINE
COOLS SUNBURN PAIN
NET WT 8 OZ( 227g)

INGREDIENTS AND APPEARANCE

SELECT BRAND BURN RELIEF 
lidocaine hcl gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15127-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15127-002-16	226 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/19/2012

Labeler - Select Brand Distributors (043562370)