ZIKS ARTHRITIS PAIN RELIEF description, usages, side effects, indications, overdosage, supplying and lots more!

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ZIKS ARTHRITIS PAIN RELIEF

Nnodum Pharmaceuticals

Arthritis Pain Relief Cream




FULL PRESCRIBING INFORMATION

Methyl Salicylate 12%, Menthol 1% and Capsaicin 0.025%

Cetyl Alcohol, Ceteth-2, Sorbitol Solution, Imidazolidinyl Urea and Purified Water.

For the temporary relief of minor aches and pain of muscles and joints associated with arthritis, simple backache, strains and sprains. *Products containing purified capsaicin are most recommended by doctors and pharmacists.

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 physician. A passing burning sensation may occur upon application, but generally disappears in several days. Application schedules of less than 3 to 4 times a day may not provide optimum pain relief ant the burning sensation may persist. WASH HANDS WITH SOAP AND WATER AFTER APPLYING UNLESS TREATING HANDS.

For external use only. Avoid contact with eyes and mucus membranes. If conditions worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. Do not apply to wounds, damage or broken (open), irritated skin or excessive irritation develops.

Do not bandage tightly. Do not use with heating pad. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product. Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

Storage

Store at room temperature 15-30 degrees C (59-86 degrees F). Lot number and expiration date: See tube seal area or end flap.

Ziks cream is supplied in a 2 oz. tube.

Distributed by: ZIKS Healthcare Products, Cincinnati, OH 45229

ZIKS ARTHRITIS PAIN RELIEF

ZIKS ARTHRITIS PAIN RELIEF

ZIKS ARTHRITIS PAIN RELIEF CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63044-030
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
methyl salicylate METHYL SALICYLATE 6.79 mg
MENTHOL 0.566 mg
capsaicin CAPSAICIN 0.014 mg

Inactive Ingredients

Ingredient Name Strength
CETYL ALCOHOL
CETETH-20
sorbitol
UREA
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63044-030-60 56.6 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 1999-11-10


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