ARTHRITIS PAIN RELIEVER- diclofenac sodium gel 
Chain Drug Consortium, LLC

----------

Diclofenac Sodium 1 percent Gel AML

Active ingredient

Diclofenac sodium (NSAID*) 1% (equivalent to 0.93% diclofenac)

* nonsteroidal anti-inflammatory drug

Purpose

Arthritis Pain Reliever

Uses

Warnings

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

  • if you have ever had an allergic reaction to any other pain reliever or to a fever reducer
  • for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries.
  • right before or after heart surgery
  • on more than 2 body areas at the same time
  • in the eyes, nose, or mouth

Ask a doctor before use if

  • you have problems or serious side effects from taking pain relievers or fever reducers
  • stomach bleeding warning applies to you
  • you have a history of stomach problems, such as heartburn
  • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
  • you are taking a diuretic
  • you are under the age of 18 years. It is not known if this drug works or is safe in children under the age of 18 years.

Ask a doctor or pharmacist before use if

  • under a doctor’s care for any serious condition
  • taking any other drug

When using this product

  • avoid contact with eyes, nose, or mouth
  • if eye contact occurs, rinse thoroughly with water

Stop use and ask a doctor if

  • pain gets worse or lasts more than 21 days
  • redness or swelling is present in the painful area
  • fever occurs
  • skin irritation occurs
  • any new symptoms appear. These could be signs of a serious condition.
  • you experience any of the following signs of stomach bleeding:
    • feel faint
    • have bloody or black stools
    • vomit blood
    • have stomach pain that does not get better
  • you have symptoms of heart problems or stroke:
    • chest pain
    • trouble breathing
    • leg swelling
    • weakness in one part of side of body
    • slurred speech

If pregnant or breast-feeding,

ask a health professional before use. It is especially important to not 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 (1-800-222-1222) right away.

Directions

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 4 times per day every day
  • Do not use on more than 2 body areas at the same time

Use ENCLOSED DOSING CARD to measure a dose

  • For each upper body area (hand, wrist, or elbow) – Squeeze out 2.25 inches (2 grams)
  • For each lower body area (foot, ankle, or knee) – Squeeze out 4.5 inches (4 grams) 

Read the enclosed User Guide for complete instructions:


Other information

Inactive ingredients

carbomer homopolymer Type C, cocoyl caprylocaprate, fragrance, isopropyl alcohol, mineral oil, polyoxyl 20 cetostearyl ether, propylene glycol, purified water, strong ammonia solution

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9 AM- 5 PM EST

Med Guide

Use enclosed dosing card to measure a dose

Diclofenac Sodium Topical Gel, 1% (NSAID) - arthritis pain reliever

Dosing Card (NOT ACTUAL SIZE)

Read product User Guide before use Not for immediate pain relief

[Upper body dose 2.25 inches long (2 grams)]

[Lower body dose 4.5 inches long (4 grams)

How to use

Principal display panel

†COMPARE TO THE ACTIVE INGREDIENT IN VOLTAREN® ARTHRITIS PAIN TOPICAL GEL

ORIGINAL PRESCRIPTION STRENGTH

Arthritis Pain Relieving Gel

DICLOFENAC SODIUM TOPICAL GEL, 1% (NSAID) 

NET WT OZ (g)

†This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC,, distributor of Voltaren® Arthritis Pain Topical Gel.

Treatment areas: Hand, Wrist, Elbow, Foot, Ankle, Knee

Not for use on any other body area (such as back, hip, or shoulder)

TAMPER EVIDENT STATEMENT: DO NOT USE IF FOIL SEAL ON TUBE OPENING IS BROKEN OR MISSING.

Distributed by: Pharmacy Value Alliance, LLC

407 East Lancaster Avenue

Wayne, PA 19087

Package Label

Diclofenac sodium (NSAID*) 1% (equivalent to 0.93% diclofenac) *non-steroidal anti-inflammatory drug

Premier Value Arthritis Pain Relieving Gel Diclofenac Sodium Topical Gel, 1% (NSAID)

ARTHRITIS PAIN RELIEVER 
diclofenac sodium gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-171
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DICLOFENAC SODIUM (UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) DICLOFENAC SODIUM10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
AMMONIA (UNII: 5138Q19F1X)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-171-501 in 1 CARTON12/31/2022
150 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:68016-171-001 in 1 CARTON12/31/2022
2100 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20807712/31/2022
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2023
Document Id: 6b29b26a-a37a-4d4b-a751-7fbf5736cf31
Set id: 8879a2ed-6c66-4489-8adc-9f160241cc7d
Version: 4
Effective Time: 20230210
 
Chain Drug Consortium, LLC