Active Ingredient
Diclofenac sodium (NSAID*) 1%
*nonsteroidal anti‑inflammatory drug
The following Structured Product Label (SPL) was submitted to the FDA by Encube Ethicals, Inc. for the product Diclofenac Sodium (NDC 21922-044). 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, do not use, ask a doctor before use if, ask a doctor or pharmacist before use if you are, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Diclofenac sodium (NSAID*) 1%
*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:
• hives • asthma (wheezing) • skin reddening • blisters • facial swelling • shock • rash
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.
ask a health professional before use. It is especially important not to use this product during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
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
|
Read the enclosed User Guide for complete instructions:
store ENCLOSED DOSING CARD with your Diclofenac Sodium Topical Gel, 1% Arthritis Pain. The dosing card is re-usable.
Carbomer homopolymer Type C, cocoyl caprylocaprate, ispropyl alcohol, mineral oil, polyoxyl 20 cetostearyl ether, propylene glycol, purified water, strong ammonia solution.
Question and comments 1-833-285-4151
Carton Label - 150 g
NDC 21922-044-26
ORIGINAL PRESCRIPTION STRENGTH
Diclofenac Sodium Topical Gel, 1%
(NSAID)- Arthritis pain reliever
For daily Treatment of Arthritis Pain Anti-Inflammatory
For external use only
Net Wt 5.29 oz (150g)
Container Label- 150 G
NDC 21922-044-26
Diclofenac Sodium Topical Gel, 1%
(NSAID)- Arthritis pain reliever
For external use only
Net Wt 5.29 oz (150g)
Dosing Card:
Use Enclosed Dosing Card to Measure a Dose
Diclofenac Sodium Topical Gel, 1%
(NSAID)- Arthritis pain reliever
Upper body dose 2.25 inches long (2 grams)
Lower body dose 4.5 inches long (4 grams)
Dosing Card (NOT ACTUAL SIZE)
* Please review the disclaimer below.