Label: ZIKS ARTHRITIS PAIN RELIEF cream
- NDC Code(s): 63044-030-60
- Packager: Nnodum Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- ACTIVE INGREDIENTS:
- ACTIVE INGREDIENTS:
- INACTIVE INGREDIENTS:
- DOSAGE & ADMINISTRATION
- INDICATIONS:
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS:
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.
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WARNING:
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.
- How Supplied:
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZIKS ARTHRITIS PAIN RELIEF
ziks arthritis pain relief creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63044-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 6.79 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.566 mg in 1 g CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.014 mg in 1 g Inactive Ingredients Ingredient Name Strength CETYL ALCOHOL (UNII: 936JST6JCN) CETETH-20 (UNII: I835H2IHHX) SORBITOL (UNII: 506T60A25R) UREA (UNII: 8W8T17847W) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63044-030-60 56.6 g in 1 TUBE; Type 0: Not a Combination Product 11/10/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/10/1999 Labeler - Nnodum Pharmaceuticals (960457273) Establishment Name Address ID/FEI Business Operations Contract Pharmacal Corporation 057795122 MANUFACTURE(63044-030)