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Sarna

Physicians Total Care, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Pramoxine hydrochloride 1%

Purpose

external analgesic

Use

for the temporary relief of itching associated with minor skin irritations

Warnings

For external use only

When using this product

  • avoid contact with the eyes.

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days.

Caution -- Do not use in the eyes or nose. Not for prolonged use. Do not apply to large areas of the body. If redness, irritation, swelling, or pain persists or increases, discontinue use unless directed by a physician.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • To open, squeeze cap tightly and turn pump counter-clockwise.

Adults and children 2 years of age and older:

  • apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: consult a doctor. 

Other Information

Side effects may be reported to 1-888-438-7426

Inactive ingredients

benzyl alcohol, carbomer 940, cetyl alcohol, dimethicone, glyceryl stearate, isopropyl myristate, PEG-8 stearate, PEG-100 stearate, petrolatum, purified water, sodium hydroxide, stearic acid

Find more about Sarna!

Stiefel Laboratories, Inc.

Research Triangle Park, NC 27709

www.sarna-skincare.com

Made in Canada

A099718

Additional barcode labeling by:
Physicians Total Care, Inc.
Tulsa, Oklahoma       74146

Principal Display Panel

NDC 54868-1587-0

Sarna®

SENSITIVE

Pramoxine Hydrochloride 1%

ANTI-ITCH LOTION

Steroid-Free and Fragrance-Free

DERMATOLOGIST Recommended

  • Relieves itching associated with:

DRY, SENSITIVE SKIN

ECZEMA

  • Moisturizing

Net Wt. 7.5 Fl Oz. (222 mL)

A099717

Sarna

Sarna

pramoxine hydrochloride LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54868-1587(NDC:0145-0630)
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
pramoxine hydrochloride PRAMOXINE 1 mg

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
CARBOMER HOMOPOLYMER TYPE C
CETYL ALCOHOL
DIMETHICONE
GLYCERYL MONOSTEARATE
ISOPROPYL MYRISTATE
POLYOXYL 8 STEARATE
POLYOXYL 100 STEARATE
petrolatum
water
SODIUM HYDROXIDE
STEARIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54868-1587-0 222 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2008-03-28


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Be sure to consult your doctor before taking any medication!
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