Active Ingredient
Diclofenac sodium (NSAID*) 1% (equivalent to 0.93% diclofenac)
*nonsteroidal anti-inflammatory drug
The following Structured Product Label (SPL) was submitted to the FDA by Exelan Pharmaceuticals Inc. for the product Diclofenac Sodium (NDC 76282-103). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children section, directions, read the enclosed user guide for compelete instructions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Diclofenac sodium (NSAID*) 1% (equivalent to 0.93% diclofenac)
*nonsteroidal anti-inflammatory drug
Arthritis pain reliever
For external use only
Allergy alert: Diclofenac may cause a severe allergic reaction, especially in people allergic to aspirin.
Symptoms may include:
If an allergic reaction occurs, stop use and seek medical help right away.
Liver warning: This product contains diclofenac. Liver damage may occur if you apply
Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is small but higher if you
Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.
Do not use
Ask a doctor before use if
Ask a doctor or pharmacist before use if you are
When using this product
Stop use and ask a doctor if
If pregnant or breast-feeding,
ask a health professional before use. It is especially important not to use diclofenac at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Use up to 21 days unless directed by your doctor
Not for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries.
| Daily | Per Dose |
|---|---|
For your arthritis pain:
| Use ENCLOSED DOSING CARD to measure a dose
|
carbomer homopolymer Type C, cocoyl caprylocaprate, fragrance, isopropyl alcohol, mineral oil, polyoxyl 20 cetostearyl ether, propylene glycol, purified water, strong ammonia solution
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Additional Information
ORIGINAL PRESCRIPTION STRENGTH
Medicated Gel Clinically Proven to Relieve Arthritis Pain
TREATMENT AREAS
Cipla
NDC 76282-103-39
Diclofenac Sodium Topical Gel, 1%
(NSAID) - Arthritis Pain Reliever
NET WT 100 g (3.53 oz)
Cipla
NDC 76282-103-39
Diclofenac Sodium Topical Gel, 1%
(NSAID) - Arthritis Pain Reliever
For Daily Treatment of Arthritis Pain
For external use only
Anti-inflammatory
NET WT 100 g (3.53 oz)
* Please review the disclaimer below.