PREDATOR- lidocaine hydrochloride cream 
Sambria Pharmaceuticals, LLC

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Drug Facts

Active Ingredient

Lidocaine HCL

Purpose

Topical Pain Reliever

Uses

Temporary relief from minor aches and pains of sore muscles and joints associated with: arthritis - backache - strains - sprains

Warnings

For external use only

Ask a doctor before you use if

you have sensitive skin, renal (kidney) and/or hepatic (liver) dysfunction

When using this product

  • Avoid contact with the eyes or mucous membranes
  • Do not apply to wounds or damaged skin
  • Do not use with other ointments, creams, sprays or liniments
  • Do not apply to irritated skin or if excessive irritation develops
  • Do not bandage
  • Wash hands after use with soap and water

If pregnant or breast-feeding

Ask a health professional before use.

Keep out of the reach of children

If accidentally ingested, get medical help or contact a Poison Control Center immediately.

Directions

  • Adults and children 6 years of age and older: Rub a thin film over affected areas not more than 4 times daily; rigorously rub product onto affected area in a circular motion for 30 to 60 seconds.
  • Children under 6 years of age: Consult a physician

Flammable

Keep away from excessive heat or open flame

Storage

Store in a cool dry place with lid closed tightly.

Inactive ingredients

Polyacrylamide and C13-14 Isoparrafin and Laureth-7, Methylsulfonylmethane, Ethoxydiglycol, Propylene Glycol, Triethanolamine, Emu Oil, Tea Tree Oil, Arnica Montana Extract, Ethylhexylglycerin, Phenoxyethanol, Isopropyl Palmitate, Stearic Acid, Glucosamine Sulfate, Chondroitin Sulfate

Questions or Comments

1-888-246-6601

Principal Display Panel

image of label

PREDATOR 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
BIS-ETHOXYDIGLYCOL SUCCINATE (UNII: YGQ120RH3I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
EMU OIL (UNII: 344821WD61)  
TEA TREE OIL (UNII: VIF565UC2G)  
ARNICA MONTANA (UNII: O80TY208ZW)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54723-100-111 in 1 CARTON12/01/201209/01/2023
1NDC:54723-100-0130 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/01/201209/01/2023
Labeler - Sambria Pharmaceuticals, LLC (078676259)

Revised: 12/2023
 
Sambria Pharmaceuticals, LLC