HomeNDC LookupIngredientsDiclofenac Sodium › 72476-0212-35
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Arthritis Pain Reliever Diclofenac sodium 10 mg/g Gel

by Care One (Retail Business Services, LLC.) · 1 TUBE in 1 CARTON (72476-212-35) / 100 g in 1 TUBE
NDC 72476-0212-35
🏷️ FDA NDC (as labeled) 72476-212-35 billing pads the product segment with a zero
This package
Contains100 g in 1 tube Pack sizes2 compare ↓
Also comes in: 50 g 72476-0212-17
OTC Generic Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Diclofenac Sodium (different manufacturers) — 3 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jan 27, 2026 — Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%. (SUN PHARMACEUTICAL INDUSTRIES INC) · FDA recall D-0342-2026
Class III · Dec 22, 2025 — Failed PH Specifications (Cipla USA, Inc.) · FDA recall D-0291-2026
Class II · Jun 22, 2023 — Defective Delivery System (ALEMBIC PHARMACEUTICALS, INC.) · FDA recall D-0941-2023
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Aug 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 72476-212-35
Product NDC 72476-212
11-digit billing NDC 72476021235
RxCUI 855633
UNII QTG126297Q
UPC 0341520005763
Application # ANDA208077
SPL Set ID 4484a332-aab1-46a9-aca8-159e7a09439f
Established class (EPC) Anti-Inflammatory Agents; Nonsteroidal Anti-inflammatory Drug
Mechanism of action Cyclooxygenase Inhibitors
Physiologic effect Decreased Prostaglandin Production
Chemical class Non-Steroidal
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Aug 2026)
Marketing start 2021-10-07
Marketing end 2026-08-28
Route TOPICAL
Dosage form GEL
Substance DICLOFENAC SODIUM
Why two NDCs? The FDA registers this code as 72476-212-35 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 72476-0212-35. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Nonsteroidal Anti-inflammatory Drug class.

Pharmacologic class Nonsteroidal Anti-inflammatory Drug
Drug family (ATC) Other dermatologicals, Acetic acid derivatives and related substances, Antiinflammatory preparations, non-steroids for topical use
How it works Cyclooxygenase Inhibitors
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerCare One (Retail Business Services, LLC.)
Application holderAMNEAL PHARMACEUTICALS
FDA applicationANDA208077 (ANDA)
Labeler code72476
First marketedOct 2021
Product typeHuman Otc Drug
Portfolio31 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
  • An actinic keratosis — often just called an AK — is a rough, scaly patch on the skin caused by years of sun exposure. These patches are considered precancerous, meaning they could...
  • What exactly is an actinic keratosis, and why do I need a prescription gel for it?
  • The typical treatment course runs 60 to 90 days of twice-daily application — that's a solid commitment, but it's necessary for the gel to do its job. Here's the thing: even after y...
  • How long do I need to use this gel, and how will I know it's working?
📖 Read our full Diclofenac guide →
1
Nutrient depletion considerations

Diclofenac Sodium may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 50 g
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
good sense arthritis pain 10 mg/g 00113-1189-01 L. 1 tube $0.083 Availability likely
Good Sense Arthritis Pain 10 mg/g 00113-8175-01 L. 1 tube $0.083 Availability likely
Diclofenac Sodium 10 mg/g 45802-0953-01 Padagis 1 tube $0.083 Availability likely
Diclofenac Sodium 10 mg/g 68001-0621-45 BluePoint 1 tube $0.083 Availability likely
Diclofenac sodium 10 mg/g 69097-0720-44 Cipla 1 tube $0.083 Availability likely
Diclofenac sodium 10 mg/g 69238-2053-01 Amneal 1 tube $0.083 Availability likely
Diclofenac Sodium 10 mg/g 70512-0106-10 SOLA 1 tube $0.083 Availability likely
Arthritis Pain 10 mg/g 70677-1125-01 Strategic 1 tube $0.083 Availability likely
Foster And Thrive Arthritis Pain 10 mg/g 70677-1293-01 Strategic 1 tube $0.083 Availability likely
Diclofenac Sodium 10 mg/g 76282-0103-39 EXELAN 1 tube $0.083 Availability likely
Arthritis Pain Reliever 10 mg/g 83324-0306-01 QUALITY 1 tube $0.083 Availability likely
Arthritis Pain Reliever 10 mg/g 46122-0752-37 AmerisourceBergen 1 tube $0.123 Availability likely
Diclofenac sodium 10 mg/g 70000-0555-01 CARDINAL 1 tube $0.123 Availability likely
Voltaren Arthritis Pain 10 mg/g 00067-8152-01 Haleon 1 tube FDA listed
Voltaren Arthritis Pain 00067-8153-01 Haleon 1 kit FDA listed
Voltaren Arthritis Pain 00067-8154-01 Haleon 1 kit FDA listed
Aleve Arthritis Pain Gel 1 mg/g 00280-0039-01 Bayer 1 tube FDA listed
Diclofenac sodium 10 mg/g 00363-1210-17 Walgreens 1 tube FDA listed
Arthritis Pain Relieving 10 mg/g 00363-3003-02 Walgreen 1 tube FDA listed
arthritis pain relieving 10 mg/g 00363-5123-01 Walgreen 1 tube Discontinued
Diclofenac Sodium Topical Gel 1% 10 mg/g 00363-7065-10 Walgreens 1 tube FDA listed
Diclofenac sodium 10 mg/g 00536-1294-31 Rugby 1 tube FDA listed
up and up arthritis pain reliever 10 mg/g 11673-0569-01 Target 1 tube FDA listed
Diclofenac Sodium 10 mg/g 11822-0870-01 Rite 1 tube FDA listed
Diclofenac sodium 10 mg/g 21130-0028-10 Safeway, 1 tube FDA listed
signature care arthritis pain 10 mg/g 21130-0313-01 Safeway 1 tube Discontinued
Diclofenac Sodium 10 mg/g 21922-0044-29 Encube 1 tube Discontinued
Diclofenac Sodium Topical Gel 1% 10 mg/g 30142-0025-10 Kroger 1 tube FDA listed
Diclofenac Sodium 10 mg/g 30142-0277-10 KROGER 1 tube FDA listed
topcare athritis pain reliever 10 mg/g 36800-0526-01 Topco 1 tube FDA listed
arthritis pain reliever 10 mg/g 37808-0087-01 H 1 tube FDA listed
equaline arthritis pain relieving 10 mg/g 41163-0087-01 United 1 tube FDA listed
Aspercreme Arthritis .01 g/g 41167-0571-00 Chattem, 1 tube FDA listed
Aspercreme Arthritis .01 g/g 41167-0573-02 Chattem, 1 tube FDA listed
arthritis pain relieving 10 mg/g 41250-0674-01 Meijer 1 tube FDA listed
CareOne arthritis pain relief 10 mg/g 41520-0788-01 American 1 tube FDA listed
arthritis pain reliever 10 mg/g 42507-0150-01 HyVee 1 tube FDA listed
Diclofenac Sodium 10 mg/g 43598-0885-10 Dr. 1 tube FDA listed
Diclofenac Sodium 10 mg/g 43598-0977-05 Dr. 1 tube FDA listed
equate arthritis pain 10 mg/g 49035-0262-01 Wal-Mart 1 tube FDA listed
Diclofenac sodium 10 mg/g 49035-0269-17 EQUATE 1 tube FDA listed
Diclofenac Sodium 10 mg/g 50090-4020-00 A-S 1 tube FDA listed
Diclofenac Sodium 10 mg/g 50090-4030-00 A-S 1 tube FDA listed
Voltaren Arthritis Pain 10 mg/g 50090-6202-00 A-S 24 tubes Discontinued
Diclofenac Sodium 10 mg/g 50090-6998-00 A-S 1 tube FDA listed
Diclofenac Sodium 10 mg/g 50090-7243-00 A-S 1 tube FDA listed
good sense arthritis pain 10 mg/g 50090-7250-00 A-S 1 tube FDA listed
Motrin Arthritis Pain 9.3 mg/g 50580-0574-01 Kenvue 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 51316-0012-15 CVS 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 51316-0073-76 CVS 1 tube FDA listed
Diclofenac Sodium Topical 10 mg/g 51316-0804-01 CVS 1 tube FDA listed
Arthritis Pain 10 mg/g 53943-0523-01 Discount 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 55319-0969-17 Family 1 tube FDA listed
Salonpas 10 mg/g 55328-0801-10 Hisamitsu 1 tube FDA listed
DG health arthritis pain 10 mg/g 55910-0424-02 Dolgencorp 1 tube FDA listed
Dg Health Arthritis Pain 10 mg/g 55910-0926-50 Dolgencorp 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 56062-0471-02 Publix 1 tube FDA listed
arthritis pain reliever 10 mg/g 56062-0878-01 Publix 1 tube FDA listed
Diclofenac Sodium 10 mg/g 57483-0185-11 INNOVUS 1 tube FDA listed
Crcle Diclofenac Sodium Topical Gel 1% 10 mg/g 57483-0596-01 Innovus 1 tube FDA listed
Diclofenac Sodium 10 mg/g 57896-0140-01 GERI-CARE 1 tube FDA listed
Diclofenac Sodium 10 mg/g 57896-0147-01 GERI-CARE 1 tube FDA listed
Diclofenac Sodium 10 mg/g 58602-0604-07 Aurohealth 1 tube FDA listed
Diclofenac Sodium 58602-0606-21 Aurohealth 1 kit FDA listed
Diclofenac Sodium 10 mg/g 58602-0609-07 Aurohealth 1 tube FDA listed
VennGel One 59088-0709-00 PureTek 1 kit FDA listed
Arthritis Pain Reliever 10 mg/g 59640-0198-01 H 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 59726-0012-50 P 1 tube FDA listed
Diclofenac Sodium 10 mg/g 62379-0401-02 Simple 1 tube FDA listed
Diclofenac Sodium 10 mg/g 63187-0753-00 Proficient 1 tube FDA listed
Diclofenac Sodium 10 mg/g 63868-0730-01 Chain 1 tube FDA listed
Diclofenac sodium 10 mg/g 63941-0812-53 Best 1 tube FDA listed
Diclofenac sodium 10 mg/g 63981-0112-15 Costco 3 tubes FDA listed
Diclofenac sodium 10 mg/g 63981-0211-15 Costco 3 tubes FDA listed
kirkland signature arthritis pain relief 10 mg/g 63981-0599-05 Costco 3 tubes FDA listed
kirkland signature arthritis pain relief 10 mg/g 63981-0799-05 Costco 3 tubes FDA listed
Diclofenac Sodium 10 mg/g 67296-2155-01 Redpharm 1 tube FDA listed
Arthritis Pain Reliever 10 mg/g 68016-0171-00 Chain 1 tube FDA listed
Diclofenac Sodium 10 mg/g 68071-2239-01 NuCare 1 tube FDA listed
Diclofenac Sodium 10 mg/g 68071-3456-01 NuCare 1 tube FDA listed
Diclofenac Sodium 10 mg/g 68071-3665-01 NuCare 1 tube FDA listed
diclofenac sodium 10 mg/g 68071-3671-01 NuCare 1 tube FDA listed
Members Mark Arthritis Pain Reliever 10 mg/g 68196-0523-05 Sam's 3 tubes FDA listed
members mark arthritis pain reliever 10 mg/g 68196-0870-05 Sam's 3 tubes FDA listed
berkley and jensen arthritis pain 68391-0205-00 BJWC 1 kit FDA listed
Diclofenac Sodium 10 mg/g 68788-7772-01 Preferred 1 tube FDA listed
Diclofenac Sodium 10 mg/g 69842-0729-01 CVS 1 tube FDA listed
Diclofenac sodium 10 mg/g 69842-0974-06 CVS 2 tubes FDA listed
Diclofenac Sodium 10 mg/g 71205-0552-00 Proficient 1 tube FDA listed
good sense arthritis pain 10 mg/g 71205-0670-00 Proficient 1 tube FDA listed
Diclofenac Sodium 10 mg/g 71205-0747-00 Proficient 1 tube FDA listed
Diclofenac Sodium 10 mg/g 72036-0014-10 Harris 1 tube FDA listed
Gencare-Arthritis Pain Relief .01 g/g 72090-0017-01 Pioneer 1 tube FDA listed
Diclofenac Sodium Gel 10 mg/g 72189-0479-01 Direct_Rx 1 g FDA listed
Amazon Basic Care Arthritis Pain 10 mg/g 72288-0624-03 Amazon.com 1 tube FDA listed
basic care arthritis pain 10 mg/g 72288-0870-01 Amazon.com 1 tube FDA listed
Arthritis Pain Reliever 10 mg/gthis 72476-0212-35 Care 1 tube Discontinued
Curist Arthritis Relief 1 g/100g 72559-0020-24 Little 1 tube FDA listed
Diclofenac sodium 10 mg/g 73469-2053-01 Scholl's 1 tube FDA listed
Diclofenac Sodium Topical 1% 1 mg/100g 73581-0104-15 YYBA 1 tube FDA listed
Diclofenac Sodium Topical Gel, 1% 1 g/100g 73715-0005-01 Mohnark 50 g Discontinued
Topcare Arthritis Pain Reliever 10 mg/g 76162-0804-01 Topco 1 tube FDA listed
Diclofenac Sodium 10 mg/g 76420-0091-01 Asclemed 100 g FDA listed
Diclofenac Sodium 10 mg/g 76420-0691-01 Asclemed 1 tube FDA listed
Arthritis Pain Relieving 10 mg/g 79481-0499-00 Meijer, 1 tube FDA listed
Equate Arthritis Pain 10 mg/g 79903-0391-01 WALMART 1 tube FDA listed
Diclofenac Sodium 10 mg/g 80425-0233-01 Advanced 1 tube FDA listed
Up And Up Arthritis Pain Reliever 10 mg/g 82442-0251-01 Target 1 tube FDA listed
Diclofenac Sodium 10 mg/g 83008-0037-00 Quality 1 tube FDA listed
Diclofenac Sodium 10 mg/g 84386-0120-01 Aurobindo 1 tube FDA listed
Diclofenac sodium 10 mg/g 85766-0136-01 Sportpharm 1 tube FDA listed
Diclofenac Sodium 10 mg/g 85766-0137-01 Sportpharm 1 tube FDA listed
Diclofenac Sodium 10 mg/g 85766-0160-01 Sportpharm 1 tube FDA listed
Arthritis Pain Relief 10 mg/g 51316-0517-00 CVS 2 tubes FDA listed
Diclofenac Sodium 10 mg/g 68788-4335-01 Preferred 1 tube FDA listed
Diclofenac sodium 10 mg/g 68071-5307-01 NuCare 1 tube FDA listed
Diclofenac Sodium 10 mg/g 68788-4135-01 Preferred 1 tube FDA listed
Diclofenac 10 mg/g 73581-0410-01 YYBA 1 tube FDA listed
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2021
On the market since
Oct 2021
📍
2026
Currently FDA-listed
5 years listed
🔓
·
Generic on the market
this product is a generic
This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Diclofenac Sodium (matched by generic name) — the program that covers self-administered drugs. 19 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Diclofenac Sodium. CMS lists 3 products for this generic; we show the highest-spend one. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$30M
Claims incl. refills
804.1K
Beneficiaries
539.2K
Spend / beneficiary
$55.63
Spend / claim
$37.30
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
72476-0212-17 1 TUBE in 1 CARTON (72476-212-17) / 50 g in 1 TUBE 2021-10-07 Discontinued by firm
72476-0212-35 You're viewing this 1 TUBE in 1 CARTON (72476-212-35) / 100 g in 1 TUBE 2021-10-07 Discontinued by firm

Pack size FAQ

What quantity is in NDC 72476-0212-35?
NDC 72476-0212-35 is listed by the FDA — 1 tube in 1 carton / 100 g in 1 tube.
What NDC number is used to bill for this package of Arthritis Pain Reliever Diclofenac sodium 10 mg/g Gel?
Bill NDC 72476-0212-35 — the 11-digit billing format is 72476021235. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 72476-212-35, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 72476-0212-35, written without dashes as 72476021235. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 72476-0212-35, the first segment (72476) is the labeler code FDA assigned to Care One (Retail Business Services, LLC.); the middle segment (0212) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (35) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 tube (72476-0212-17). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Care One (Retail Business Services, LLC.) is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage 53 words

Uses for the temporary relief of arthritis pain ONLY in the following areas: hand, wrist, elbow (upper body areas) foot, ankle, knee (lower body areas) this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use

⏱️ Dosage and Administration 184 words

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: use only as directed do not use more than directed or for longer than directed apply only to clean, dry skin that does not have any cuts, open wounds, infections, or rashes do not apply in same areas as any other product do not apply with external heat such as a heating pad do not apply a bandage over the treated area store ENCLOSED DOSING CARD with your Diclofenac Sodium Topical Gel, 1%.

The dosing card is re-usable.

⚠️ Warnings ~2 min read

Warnings 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: more or for a longer time than directed when using other drugs containing diclofenac Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is small but higher if you: are age 60 or older have had stomach ulcers or bleeding problems take a blood thinning (anticoagulant) or steroid drug take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others) have 3 or more alcoholic drinks every day while using this product apply more or for longer than directed 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 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.

🧪 Active Ingredient 14 words

Active ingredient Diclofenac sodium (NSAID*) 1% (equivalent to 0.93% diclofenac) * nonsteroidal anti-inflammatory drug

🧪 Inactive Ingredients 24 words

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

🎯 Purpose 4 words

Purpose Arthritis Pain Reliever

💬 Medication Guide 95 words

Med Guide 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)] Dosing Card (NOT ACTUAL SIZE) [Lower body dose 4.5 inches long (4 grams) Read product User Guide before use Not for immediate pain relief How to use For arthritis pain only Use 4 times a day May take up to 7 days to work for your arthritis pain For use on no more than 2 body areas Use up to 21 days unless directed by a doctor

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.