Predator description, usages, side effects, indications, overdosage, supplying and lots more!

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Predator

Sambria Pharmaceuticals, LLC

Predator


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Purpose

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.

Predator 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

Predator

Lidocaine Hydrochloride CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54723-101
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE LIDOCAINE 400 mg

Inactive Ingredients

Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:54723-101-02 400 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-02-11


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Be sure to consult your doctor before taking any medication!
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