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Predator by Sambria Pharmaceuticals, LLC

Medically reviewed on March 13, 2018

Dosage form: cream
Ingredients: LIDOCAINE HYDROCHLORIDE 400mg in 1mg
Labeler: Sambria Pharmaceuticals, LLC
NDC Code: 54723-101

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.

Predator

For external use only

Avoid contact with eyes

If symptoms persist for more than seven days, or clear up and occur again within a few days, discontinue use and consult physician

If redness, irritation, swelling, pain or ot5her symptoms increase, discontinue use and consult physician

If swallowed consult physician.

active ingredients

lidocaine HCL 4%

Other ingredients

Aqua, Amica Montana Extract, C13-14 Isoparafin, Chondrotin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth 7, Melaleuca Alternifoil (Tea Tree) oil, Methylsulfonylmethana (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine

Keep out of reach of children

External anesthetic

For adults and children two years or older, apply externally to the affected area. Do not use more than three to four times per day.

Uses

For temporary relief of pain and itching and minor skin irratations due to minor cuts and scrapes, sunburn and minor burns. Also used for temporary relief of itching associated with minor skin irritations and rashes due to insect bites, poison ivy, poison oak and poison sumac, soaps, detergetns, cosmetics and jewelry.

PREDATOR 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-101
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE400 mg  in 1 mg
Inactive Ingredients
Ingredient NameStrength
WATER 
ARNICA MONTANA FLOWER 
C13-14 ISOPARAFFIN 
CHONDROITIN SULFATE (BOVINE) 
EMU OIL 
DIETHYLENE GLYCOL MONOETHYL ETHER 
ETHYLHEXYLGLYCERIN 
GLUCOSAMINE SULFATE 
ISOPROPYL PALMITATE 
LAURETH-7 
TEA TREE OIL 
DIMETHYL SULFONE 
PHENOXYETHANOL 
POLYACRYLAMIDE (10000 MW) 
PROPYLENE GLYCOL 
STEARIC ACID 
TRIETHANOLAMINE BENZOATE 
Packaging
#Item CodePackage Description
1NDC:54723-101-02400 mg in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/11/2013
Labeler - Sambria Pharmaceuticals, LLC (078676259)
Establishment
NameAddressID/FEIOperations
Pure Source969241041manufacture(54723-101)

 
Sambria Pharmaceuticals, LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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