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Pain Relieving Trolamine Salicylate 100 mg/g Cream — NDC 70000-0744-01 package photo

Pain Relieving Trolamine Salicylate 100 mg/g Cream

by CARDINAL HEALTH 110, LLC. DBA LEADER · 1 TUBE in 1 CARTON (70000-0744-1) / 85 g in 1 TUBE
NDC 70000-0744-01
🏷️ FDA NDC (as labeled) 70000-0744-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 70000-0744-1
Product NDC 70000-0744
11-digit billing NDC 70000074401
RxCUI 313518
UNII H8O4040BHD
Application # M017
SPL Set ID b813262e-57c6-4d2c-8cc0-7a17f6f59343
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-12-04
Route TOPICAL
Dosage form CREAM
Substance TROLAMINE SALICYLATE
Why two NDCs? The FDA registers this code as 70000-0744-1 — a 5-4-1 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 package segment → 70000-0744-01. 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.

🏭 Manufacturer & labeler

LabelerCARDINAL HEALTH 110, LLC. DBA LEADER
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code70000
First marketedDec 2025
Product typeHuman Otc Drug
Portfolio163 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

🧪 What is this product?

This is an over-the-counter topical cream containing trolamine salicylate, a pain-relieving agent. Applied directly to the skin, trolamine salicylate is typically used to help reduce minor muscle and joint pain and discomfort. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for its product category rather than undergoing individual product review.

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.

💊 What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 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 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • 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 A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII B7862WZ632
    Potassium phosphate is a mineral salt that acts as a buffer and pH control agent in medicines. It helps keep the medication at the right acidity level for stability and proper absorption.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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.

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

The official label also statesaloe barbadensis leaf extract, cetyl alcohol, glycerin, methylparaben, mineral oil, potassium phosphate, propylparaben, sodium hydroxide, stearic acid, water.

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.

💲 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 $0.034 $2.92 / 85 g
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.
NADAC price history (per g) — tap or hover for the price & month
Jul 2026 $0.034 $0.034
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
Pain Relieving 100 mg/gthis 70000-0744-01 CARDINAL 1 tube $0.034 — Availability likely —
Mobisyl 10 g/100g 00225-0360-11 BF 100 g — — FDA listed —
Walgreens Pain Relieving Plus Turmeric Analgesic 100 mg/g 00363-3630-01 Walgreen 1 tube — — FDA listed —
Aspercreme Pain Relieving 10 g/100g 41167-0570-01 Chattem, 1 tube — — Discontinued —
Meijer Analgesic with Aloe Topical Analgesic 100 mg/g 41250-0418-01 Meijer 1 tube — — FDA listed —
Arthritis Relief GoodSense 10 g/100g 50804-0207-03 Geiss, 1 tube — — FDA listed —
Arthritis Cream 10 g/100g 51316-0990-10 CVS 85 g — — FDA listed —
Jointiva 10 g/100g 57237-0355-85 Rising 1 tube — — FDA listed —
Pain Relief Cream 100 mg/g 62742-4091-01 ALLURE 57 g — — FDA listed —
Blue-Emu Maximum Pain Relief .1 g/g 69993-0300-03 Kingsway 88 g — — FDA listed —
Tommie Copper Pain Relief Maximum Strength 10 g/100g 72562-0103-03 Tommie 85 g — — FDA listed —
Tommie Copper Pain Relief 10 g/100g 72562-0223-25 Tommie 70 g — — FDA listed —
Warrior Arthritis Relief 10 g/100g 72839-0213-03 Derma 1 tube — — FDA listed —
DCH Arthritis Relief 10 g/100g 72839-0214-03 Derma 1 tube — — FDA listed —
Equate Odor-Free Therapy Arthritis Analgesic 100 mg/g 79903-0117-01 Wal-Mart 1 tube — — FDA listed —
Dermachange Arthritis Relief 10 g/100g 83520-0214-03 Private 1 tube — — FDA listed —
CBD Pain Relief Cream 100 mg/g 62742-4198-01 Allure 57 g — — 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

🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70000-0744-01 You're viewing this 1 TUBE in 1 CARTON (70000-0744-1) / 85 g in 1 TUBE 2025-12-04 Active

📄 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
🎯 Indications and Usage 17 words ▾

Uses for the temporary relief of minor aches and pains associated with simple backache, arthritis, and sprains.

⏱️ Dosage and Administration 34 words ▾

Directions Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily. children under 12 years of age: do not use, consult a doctor

⚠️ Warnings ~1 min read ▾

Warnings For external use only Allergy alert if prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product • avoid contact with the eyes • do not use at the same time as other topical analgesics • do not apply to wounds or damaged skin • do not bandage tightly • do not use with heating pads or other heating devices. • Use only as directed. Read and follow all directions and warnings.

Stop use and ask a doctor • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days • redness is present • irritation develops. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately. Allergy alert! If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

When using this product use only as directed. Read an follow all directions and warnings on this label do not bandage tightly or apply local heat (such as heating pads) to the area of use avoid contact with eyes and mucous membranes do not apply to wounds or damaged, broken or irritated skin do not use at the same time as other topical analgesics Stop use and consult a doctor if condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days redness is present irritation develops If you are pregnant or nursing a baby , seek the advice of a health professional before using this product.

Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

🧪 Active Ingredient 4 words ▾

Active ingredients Trolamine Salicylate

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients aloe barbadensis leaf extract, cetyl alcohol, glycerin, methylparaben, mineral oil, potassium phosphate, propylparaben, sodium hydroxide, stearic acid, water.

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70000-0743-01 · Leader/ 70000-0745-01 · LEADER/ →
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.