Res-Q Analgesic Topical Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Res-Q Analgesic Topical Pain Relief

CONAIR CORPORATION

Res-Q Analgesic Topical Pain Relief Spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Res-Q Analgesic Topical Pain Relief Spray

Active Ingredient

Lidocaine Hydrochloride 4%

Purpose

Topical Analgesic

Uses:

For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

Directions:

Adult use only: Shake well. Apply (spray) onto affected area not more than 3-4 times daily.

Inactive Ingredients:

Water, urea, isopropyl palmitate, PEG-8, Polysorbate 80, dimethicone, phenoxyethanol, sodium hydroxide, propylene glycol, allantoin, carbomer, cetrimonium bromide, diazolidinyl urea, lecithin, iodopropyl butylcarbamate.

Warnings

For external use only.

Stop use and consult a doctor immediately if you experience weakness; confusion; headache; difficulty breathing; pale, grey or blue-colored skin, lips, or nail beds or any other unusual symptoms.

Do not use more than the recommended dose.

Do not cover the treated area with a dressing or bandage.

Children should be closely observed during and after use of this product as they are at greater risk for serious side effects.

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

Discontinue use and consult a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Seek immediate medical attention if ingested.

Keep away from mouth and eyes.

If contact occurs, rinse thoroughly with water.

Keep away from children. Do not use on children under 14.

Res-Q Analgesic Topical Pain Relief Spray 2oz/60ml

Res-Q Analgesic Topical Pain Relief

Res-Q Analgesic Topical Pain Relief

LIDOCAINE HYDROCHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:12829-2001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE HYDROCHLORIDE LIDOCAINE 40 mg

Inactive Ingredients

Ingredient Name Strength
water
UREA
ISOPROPYL PALMITATE
polyethylene glycol 400
polysorbate 80
DIMETHICONE
PHENOXYETHANOL
SODIUM HYDROXIDE
propylene glycol
ALLANTOIN
CETRIMONIUM BROMIDE
DIAZOLIDINYL UREA
EGG PHOSPHOLIPIDS
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:12829-2001-0 60 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-02-26


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