KROGER BURN RELIEF ALOE- lidocaine hydrochloride gel 
THE KROGER CO

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.

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Drug Facts

Active ingredient

Lidocaine HCl 0.50%

Purpose

Topical Anesthetic

Uses

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.

Stop use and ask a doctor if

  • Conditions worsens or symptoms persists for more than 7 days.
  • Symptoms 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

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.

Principal Display Panel

Kroger

QUALITY GUARANTEED

Aloe Vera
Burn
Relief
Gel
with LIDOCAINE

Cools Sunburn Pain

NET WT 8 OZ (226 g)
Z38487A0.jpg
KROGER  BURN RELIEF ALOE
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-900
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30142-900-16226 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/19/2012
Labeler - THE KROGER CO (006999528)

Revised: 11/2012
Document Id: 948785e9-ff77-4008-abee-7797200390b8
Set id: a4c58147-7dc5-4c27-83e9-ee6abaad58fc
Version: 1
Effective Time: 20121119
 
THE KROGER CO