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Jointflex Camphor 3.2 g/100g Cream — NDC 72927-0944-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Jointflex Camphor 3.2 g/100g Cream — NDC 72927-944-03 (Billing 72927-0944-03)

by Strides Consumer LLC · 1 TUBE in 1 CARTON / 28 g in 1 TUBE

This is a package of Jointflex Camphor 3.2 g/100g Cream from Strides Consumer LLC, marketed since Mar 2020 and currently FDA-listed.

NDC 72927-0944-03
🏷️ FDA NDC (as labeled) 72927-944-03 billing pads the product segment with a zero
This package
Contains28 g in 1 tube Pack sizes3 compare ↓
Product page 72927-0944-01 Also comes in: 85 g 72927-944-01 28 g 72927-944-02
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 72927-944-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72927 labeler · 944 product · 03 package
Package marketed since
Mar 26, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0372917000245
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72927-944-03
Product NDC 72927-944
11-digit billing NDC 72927094403
RxCUI 2181415, 2282659
UNII 5TJD82A1ET
UPC 0372917000245
Application # M017
SPL Set ID 766b73f2-67bd-4d5c-805c-1057b3981ebf
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-03-09
Route TOPICAL
Dosage form CREAM
Substance CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 2181415
Why two NDCs? The FDA registers this code as 72927-944-03 — 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 → 72927-0944-03. 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.

Clinical

🧪 What is this product?

Jointflex Camphor is an over-the-counter topical cream containing synthetic camphor at a 3.2 percent concentration. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of product rather than undergoing individual FDA review. Camphor in topical creams is typically used to produce a warming or cooling sensation on the skin and may be included in products intended for temporary relief of minor muscle and joint discomfort. The cream is applied directly to the skin over the affected area.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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: 85 g 28 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
72927-0944-01 72927-944-01 Main listing 1 TUBE in 1 CARTON / 85 g in 1 TUBE 2020-03-09 — Active
72927-0944-02 72927-944-02 1 TUBE in 1 CARTON / 28 g in 1 TUBE 2021-09-01 — Active
72927-0944-03 You're viewing this 1 TUBE in 1 CARTON / 28 g in 1 TUBE 2021-03-26 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 carton / 28 g in 1 tube.
What NDC number is used to bill for this package of Jointflex Camphor 3.2 g/100g Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Jointflex 3.2 g/100g 72927-0904-01 Strides 1 tube — — FDA listed —
Jointflex 3.2 g/100gthis 72927-0944-03 Strides 1 tube — — FDA listed —
Jointflex 3.2 g/100g 72927-0976-02 Strides 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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

🏛️
2020
On the market since
Mar 2020
📍
2026
Currently FDA-listed
6 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

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.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 2X654GD19H
    Acetylated lanolin is a waxy substance derived from sheep's wool that has been chemically modified. It serves as an emollient and lubricant in medicines, helping to soften formulations and improve how they spread or are absorbed.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 809Y72KV36
    A synthetic polymer made from acrylic acid and crosslinked with allyl pentaerythritol. It's used as a thickening agent and gelling ingredient in creams, gels, and lotions to create the proper texture and help the medicine spread and stay on the skin.
  • UNII 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • UNII 2ZAJ1K50XH
    A naturally derived compound extracted from shark cartilage, used as a binder and thickening agent in tablet and capsule formulations to help hold ingredients together and control product texture.
  • UNII H5RIZ3MPW4
    A chemical preservative used to prevent bacterial and fungal growth in medicines. It helps extend shelf life and maintain product safety during storage and use.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII 15VQ11I66N
    Glucosamine sulfate potassium chloride is a compound combining glucosamine, a natural sugar, with sulfate and potassium chloride salts. It may serve as an active ingredient or structural component in formulations, helping stabilize the product and support consistency.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII EOI0B9800C
    A waxy substance derived from sheep's wool that has been chemically modified to improve its properties. Used as an emollient, emulsifier, and thickener in creams and ointments to help blend oil and water ingredients and soften the product.
  • UNII 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • UNII 603P14DHEB
    A synthetic antimicrobial chemical used as a preservative in topical and cosmetic formulations. It prevents bacterial and fungal growth in products to maintain stability and safety during storage and use.
  • UNII J3QD0LD11P
    A synthetic compound made by combining glucose with methyl alcohol and polyethylene glycol. It acts as an emulsifier and solvent to help blend water and oil-based ingredients and improve how the medicine dissolves or spreads.
  • UNII V1YW10H14D
    A waxy substance made from glucose and stearic acid that acts as an emulsifier and thickener in medicines, helping to blend ingredients together and create a smooth, stable texture in creams and ointments.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • UNII 13A4J4NH9I
    A synthetic emulsifier derived from stearic acid and polyethylene glycol. It helps mix oil and water-based ingredients together in liquid medicines and creams to create a smooth, uniform product.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII D2YCN1I522
    Shark cartilage is a natural material derived from shark skeletal tissue. In medications, it acts as a filler and binder to help form tablets and capsules while providing bulk and structure to the dose.
  • UNII 6KGS8SP16U
    A natural essential oil from turmeric root that gives medicines a yellow color and mild spice flavor. It's used mainly as a colorant and flavoring agent in tablets, capsules, and liquid formulations.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

26 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAcetylated Lanolin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera, C12-15 Alkyl Benzoate, Chondroitin Sulfate, Diazolidinyl Urea, Dimethicone, Dimethiconol Stearate, Disodium EDTA, DL Panthenol, Glucosamine Sulfate, Glycerin, Glycerol Stearate, Glycosaminoglycans, Hydroxylated Lanolin, Hydroxpropyl Methycellulose, Iodopropynyl Butylcarbamate, Methyl Gluceth-20, Methyl Glucose Sesquistearate, Peppermint Oil, Polysorbate 20, Potassium Carbomer, Purified Water, Tocopheryl Acetate (Vitamin E), Turmeric (Oil & Oleoresin).

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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.

Manufacturer & labeler

LabelerStrides Consumer LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code72927
First marketedMar 2020
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Strides Consumer LLC labeler code 72927

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.

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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 22 words ▾

Uses: For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

⏱️ Dosage and Administration 71 words ▾

Directions: adults and children 12 years of age and older: clean, rinse and dry skin prior to application apply generously to painful muscles and joints, gently massaging until the JointFlex ® Pain Relieving Cream disappears repeat as necessary, but no more than 4 times a day for optimum benefit, use daily for at least two weeks and continue to use daily thereafter children under 12 years of age: ask a doctor

⚠️ Warnings 5 words ▾

Warnings: For external use only.

🧪 Active Ingredient 4 words ▾

Active ingredient Camphor (3.2%)

🧪 Inactive Ingredients 57 words ▾

Inactive ingredients: Acetylated Lanolin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera, C12-15 Alkyl Benzoate, Chondroitin Sulfate, Diazolidinyl Urea, Dimethicone, Dimethiconol Stearate, Disodium EDTA, DL Panthenol, Glucosamine Sulfate, Glycerin, Glycerol Stearate, Glycosaminoglycans, Hydroxylated Lanolin, Hydroxpropyl Methycellulose, Iodopropynyl Butylcarbamate, Methyl Gluceth-20, Methyl Glucose Sesquistearate, Peppermint Oil, Polysorbate 20, Potassium Carbomer, Purified Water, Tocopheryl Acetate (Vitamin E), Turmeric (Oil & Oleoresin).

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Do Not Use 18 words ▾

Do not use if skin is irritated or damaged excessive irritation develops 12 years of age or under

📄 Ask a Doctor Before Use If 13 words ▾

Ask a doctor before use if you have redness over the affected area

📄 When Using This Product 38 words ▾

When using this product use only as directed avoid contact with the eyes and mucous membranes do not apply to wounds, damaged, broken or irritated skin do not bandage tightly or use a heating pad do not swallow

📄 Stop Use and Ask a Doctor If 27 words ▾

Stop use and ask doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness develops

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 20 words ▾

Other information store at room temperature with the cap closed notice: because this product contains natural nutrients, color may vary

📄 Questions or Comments 52 words ▾

Questions or comments? Call (866) 235-4581 or email [email protected] Manufactured for Strides Consumer LLC, East Brunswick, NJ 08816 Licensed user of trademarks. © 2020 Strides Consumer LLC †Results based on a 2021 Healthcare Provider survey conducted by InStep Health as part of a point-of-care marketing campaign sponsored by Strides Consumer LLC. www.jointflex.com

📄 Package Label / Principal Display Panel ~2 min read ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL 8 Week Challenge for pain relief* #1 CLINICALLY RECOMMENDED† JOINT PAIN CREAM JointFlex ® - Pain Relief Cream with natural Turmeric Effectively Reduces Joint Pain Immediate & Long Lasting Relief* Contains Glucosamine & Chondroitin** No stain/ No Grease/ Pleasant Scent NET WT 3 OZ (85g) DEEP PENETRATING Fusome ® Technology Quick & effective penetration Targeted pain relief Long lasting relief when used daily Flex Your Freedom ™ Relieves Back, Neck, Shoulder, Knees, Elbow, Foot, Ankle, Leg Hand and Wrist pain NDC 72927-944-01 Visit www.jointflex.com for more information * when applied as directed ** For skin conditioning 011-1630C-R02 8 Week Challenge for pain relief* 100% Money Back Guarantee* Effectively Reduces Joint Pain JointFlex ® - Pain Relief Cream with natural Turmeric Immediate & Long Lasting Relief* Contains Glucosamine & Chondroitin** No stain/ No Grease/ Pleasant Scent DEEP PENETRATING Fusome ® Technology Quick & effective penetration Targeted pain relief Long lasting relief when used daily Flex Your Freedom ™ Relieves Back, Neck, Shoulder, Knees, Elbow, Foot, Ankle, Leg Hand and Wrist pain NET WT 1 OZ (28g) JointFlex ® GUARANTEE "If you use JointFlex as directed and are not completely amazed with the pain relief you received, simply return the tube (even if it's empty) and the cash register receipt to the address below for a full refund.

No questions asked." Questions or comments? Call (866)-235-4581. Strides Consumer LLC, East Brunswick, NJ 08816 NDC 72927-944-03 Visit www.jointflex.com for more information Licensed user of trademarks. © 2020 Strides Consumer LLC Sample not for retail sale. * when applied as directed ** For skin conditioning 8 Week Challenge for pain relief* 100% Money Back Guarantee* Effectively Reduces Joint Pain JointFlex ® - Pain Relief Cream with natural Turmeric Immediate & Long Lasting Relief* Contains Glucosamine & Chondroitin** No stain/ No Grease/ Pleasant Scent DEEP PENETRATING Fusome ® Technology Quick & effective penetration Targeted pain relief Long lasting relief when used daily Flex Your Freedom ™ Relieves Back, Neck, Shoulder, Knees, Elbow, Foot, Ankle, Leg Hand and Wrist pain NET WT 1 OZ (28g) JointFlex ® GUARANTEE "If you use JointFlex as directed and are not completely amazed with the pain relief you received, simply return the tube (even if it's empty) and the cash register receipt to the address below for a full refund.

No questions asked." Questions or comments? Call (866)-235-4581. Strides Consumer LLC, East Brunswick, NJ 08816 NDC 72927-944-02 Visit www.jointflex.com for more information Licensed user of trademarks. © 2020 Strides Consumer LLC * when applied as directed ** For skin conditioning Jointflex turmeric - 3 OZ 28g Carton image Carton-1oz-for sale

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Jointflex (this brand).

Top reported reactions

Fatigue31
Pain30
Drug Hypersensitivity29
Pruritus27
Dyspnoea25
Erythema25
Headache24

Age at onset

Neonate1
Infant1
Adolescent1
Adult20
Elderly16

Reporter sex

176 reports
Male · 38%
Female · 62%

Serious outcomes

Hospitalization77
Death14
Life-threatening9
Disabling7
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 33 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
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 ✓ Available
Inactive ingredients (structured) ✓ 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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
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.
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Strides Consumer LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 tube (72927-0944-01), 1 tube (72927-0944-02). 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?
Strides Consumer 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.
← 72927-0904-01 · Strides 72927-0976-02 · Strides →
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.