Diclofenac Sodium Gel
Product Images NDC 21922-044

9 FDA label images from Encube Ethicals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 21922-044). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Encube Ethicals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Cc 100

Cc 100
Packaging label for Diclofenac Sodium Topical Gel, 1% (10 mg/g), an NSAID arthritis pain reliever by Encube Ethicals Private Limited. The label includes dosage instructions with a dosing card guide, usage directions for arthritis pain, treatment areas (hand, wrist, elbow, foot, ankle, knee), and a net weight of 3.53 oz (100 g). It features tamper-evident warnings and emphasizes use for up to 21 days unless directed otherwise.*
FDA Label Image

Cc 150

Cc 150
Diclofenac Sodium Topical Gel, 1% (10 mg/g) in a 5.29 oz (150 g) net weight tube, labeled as an arthritis pain reliever NSAID. The packaging includes dosing instructions with a dosing card measuring upper and lower body doses. It displays treatment area icons (hand, wrist, elbow, foot, ankle, knee) and manufacturer information for Encube Ethicals Private Limited. The box includes usage directions, warnings, and a barcode.*
FDA Label Image

Cc 20

Cc 20
Packaging label for Diclofenac Sodium Topical Gel, 1% (10 mg/g), an NSAID arthritis pain reliever by Encube Ethicals Private Limited. The label states a net weight of 0.7 oz (20 g) and includes dosing instructions, treatment areas (hand, wrist, elbow, foot, ankle, knee), and a tamper-evident statement. It also features directions for use and warnings.*
FDA Label Image

Cc 50

Cc 50
Packaging label for Diclofenac Sodium Topical Gel 1%, an NSAID arthritis pain reliever by Encube Ethicals Private Limited. The label displays the product name, strength, and uses for arthritis pain. It includes directions for use, treatment areas (hand, wrist, elbow, foot, ankle, knee), and dosing instructions. The net weight is 1.76 oz (50 g). The label features a tamper-evident statement, manufacturer and distributor information, and a barcode with NDC 21922-044-14.*
FDA Label Image

Dosing

Dosing
A dosing card panel for Diclofenac Sodium Topical Gel, 1%, NSAID arthritis pain reliever. It provides upper body dose instructions of 2.25 inches (2 grams) and lower body dose instructions of 4.5 inches (4 grams). It advises reading the user guide before use and states the product is not for immediate pain relief.*
FDA Label Image

Tl 100

Tl 100
Diclofenac Sodium Topical Gel 1% carton label from Encube Ethicals Private Limited. The label states it is a 100 g tube (3.53 oz) with arthritis pain reliever (NSAID) designation. It includes usage instructions, warnings, tamper-evident information, and a barcode with NDC 21922-044-09.*
FDA Label Image

Tl 150

Tl 150
Diclofenac Sodium Topical Gel, 1%, 10 mg/g, in a 150 g tube by Encube Ethicals Private Limited. The label indicates use as a nonsteroidal anti-inflammatory drug (NSAID) for arthritis pain relief. It includes warnings, usage instructions, and a barcode.*
FDA Label Image

Tl 20

Tl 20
Diclofenac Sodium Topical Gel 1% tube packaging label by Encube Ethicals Private Limited. The label highlights the product as an NSAID arthritis pain reliever with a net weight of 0.7 oz (20 g). It includes directions for use, warnings such as stomach bleeding risk, and storage instructions. The label also features a barcode and manufacturer details.*
FDA Label Image

Tl 50

Tl 50
The packaging label for Diclofenac Sodium Topical Gel, 1%, by Encube Ethicals Private Limited. The label states it is a 50 g tube (1.76 oz) and identifies the product as an NSAID arthritis pain reliever. Directions mention unscrewing the cap to open and warnings cover stomach bleeding, allergy alerts, and safe use instructions. A barcode and NDC 21922-044-14 appear on the label.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.