Sunmark Camphor Spirit description, usages, side effects, indications, overdosage, supplying and lots more!

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Sunmark Camphor Spirit

McKesson

Sunmark Camphor Spirit USP


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION


Drug Facts

Active Ingredient

Camphor 10%

Purpose

Counterirritant

Use

For the temporary relief of minor aches, muscle and joint pain associated with arthritis, strains, brusies and simple backache.

Warnings

For external use only.

Do not drink. If swallowed, immediately give 3 or 4 glases of water. Do not induce vomiting. If vomiting occurs, give fluids again. Do not give anything by mouth to an unconscious or convulsing person. Get medical attention immediately.

Avoid contact with eyes or mucous membranes.

Do not apply to irritated skin.

When using this product

Do not bandage tightly.

Discontinue use and consult a doctor if

condition worsens, or if excesive irritation develops.

symptoms persit for more than 7 days, or clear up and occur again within a few days.

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away. In case of eye contact, flush eyes with running water for 15 minutes, get medical attention.

Directions

(dilute 3 parts olive oil and mix well)

Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily.

Children under 2 yrs of age: consult a doctor befre use.

Other Information

Flammable: Keep away from spark, heat and flame.

Inactive ingredients

Alcohol 84%, Purified Water

Questions or Comments?

1-800-662-3435

Principal Display Panel

Camphor Spirits, USP

Sunmark Camphor Spirit

Sunmark Camphor Spirit

Camphor 10% LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-148
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (NATURAL) 100 mg

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-148-30 59 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2008-01-01


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Be sure to consult your doctor before taking any medication!
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