LIDOCIN- lidocaine hydrochloride gel 
Pharmaceutics Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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For external use only

Avoid contact with eyes

Do not applly to open wounds or damaged skin

If symptoms persist for more than seven days, discontinue use and consult physician

If swallowed, consult physician

Do not bandage tightly

If pregnant or breast feeding, contact physician prior to use

Do not use in large quantities, particularly over raw surfaces or blistered areas

Keep out of reach of children

Lidocaine HCL 3.00%

aloe barbadensis leaf, water, arnica montan extract, boswella serrata extract, camelia sinensis leaf extract, carbomer, ethylhexylglycerine, glycerine, isopropyl myristate, PEG 8, phenoxyethanol, polysorbate 80, sodium lauryl sulfate, triethanolamine, fd&c blue #1, fd&c yellow #5

Directions

Apply directly to effected area. Do not use more than four times per day.

For temporary relief of pain associated with minor cuts, scrapes and minor skin irritations

label

LIDOCIN 
lidocaine hcl gel
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:49430-050
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.9 g  in 30 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARNICA MONTANA (UNII: O80TY208ZW)  
BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)  
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
MAGNESIUM SULFATE (UNII: DE08037SAB)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49430-050-3030 g in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/20/201510/15/2015
Labeler - Pharmaceutics Corporation (079132026)
Establishment
NameAddressID/FEIBusiness Operations
Zhuhai Guojia New Macromolecule Material Co., LTD679871251manufacture(49430-050)

Revised: 9/2015
 
Pharmaceutics Corporation