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Red Cross Toothache eugenol 850 mg/mL Liquid, 1 bottle — NDC 10742-0009-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Red Cross Toothache eugenol 850 mg/mL Liquid, 1 bottle — NDC 10742-0009-1 (Billing 10742-0009-01)

by The Mentholatum Company · 1 BOTTLE in 1 BLISTER PACK / 3.7 mL in 1 BOTTLE

This is a package of 1 bottle of Red Cross Toothache eugenol 850 mg/mL Liquid from The Mentholatum Company, marketed since Jun 1983 and currently FDA-listed. It is this product's only package size.

NDC 10742-0009-01
🏷️ FDA NDC (as labeled) 10742-0009-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 10742-0009-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
10742 labeler · 0009 product · 1 package
Package marketed since
Jun 21, 1983
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 1074200091 7
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 10742-0009-1
Product NDC 10742-0009
11-digit billing NDC 10742000901
UNII 3T8H1794QW
Application # M022
SPL Set ID 3537e599-65d9-48d6-8a46-d42312f71e84
Established class (EPC) Standardized Chemical Allergen
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1983-06-21
Route TOPICAL
Dosage form LIQUID
Substance EUGENOL

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 002630
GCN 14900
HICL code 001130
Ingredient (HICL) Eugenol
HIC1 code D
Therapeutic class — broad (HIC1) Biliary System/Gastro-Intestinal System
HIC2 code D2
Therapeutic class — intermediate (HIC2) Drugs Acting On Teeth
HIC3 code D2D
Therapeutic class — specific (HIC3) Tooth Ache Preparations
AHFS code 52:16.00.00
AHFS class Local Anesthetics (Eent)
FDB label name RED CROSS TOOTHACHE KIT
FDB brand name Red Cross Toothache Kit
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 002630
  • GCN: 14900
  • HICL (First Databank): 001130
  • AHFS class code: 52:16.00.00
Why two NDCs? The FDA registers this code as 10742-0009-1 — 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 → 10742-0009-01. 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.

Clinical

Label name RED CROSS TOOTHACHE KIT Ingredient Eugenol
🧪 What is this product?

Red Cross Toothache is a topical liquid containing eugenol, a natural compound from clove oil. It is an over-the-counter monograph product typically used for temporary relief of minor toothache pain when applied directly to the affected tooth or gum area. Eugenol has numbing properties that are commonly used in dental care products for this purpose.

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 mLPer 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.
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
10742-0009-01 You're viewing this Main listing 1 BOTTLE in 1 BLISTER PACK / 3.7 mL in 1 BOTTLE 1983-06-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Red Cross Toothache 850 mg/mLthis 10742-0009-01 The 1 bottle — — 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

🏛️
1983
On the market since
Jun 1983
📍
2026
Currently FDA-listed
43 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 QX10HYY4QV
    Sesame oil is a plant-derived oil from sesame seeds. It's used in medicines as a solvent or carrier to dissolve or suspend active ingredients, helping them mix evenly throughout the formulation.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statessesame oil

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

LabelerThe Mentholatum Company
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code10742
First marketedJun 1983
Product typeHuman Otc Drug
Portfolio108 products on file

More NDCs from The Mentholatum Company labeler code 10742

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Uses temporarily relieves throbbing, persistent toothache due to a cavity until a dentist can be seen

⏱️ Dosage and Administration 82 words ▾

Directions rinse tooth with water to remove any food particles from the cavity using tweezers, immerse cotton pellet in medication to prevent dripping , squeeze gently between fingers to remove excess liquid place pellet in tooth cavity for one minute without touching surrounding tissues , then remove supervise children using this product adults and children 12 years and over: use up to 4 times daily or as directed by a dentist or doctor children under 12 years: ask a dentist or doctor

⚠️ Warnings 115 words ▾

Warnings For external use only Allergy alert: do not use if you are allergic to eugenol (clove oil) When using this product use only in teeth with persistent, throbbing pain avoid touching tissues other than tooth cavity. Contact with lips or mucous membranes can cause burning, swelling, or irritation. DO NOT SWALLOW to avoid irritation do not use for more than 7 days do not exceed recommended dosage Stop use and ask a dentist or doctor if irritation persists, inflammation develops, or if fever and infection develop See a dentist as soon as possible whether or not the pain is relieved.

Toothaches and open cavities indicate serious problems that need prompt attention by a dentist.

🧪 Active Ingredient 4 words ▾

Active ingredient Eugenol 85%

🧪 Inactive Ingredients 4 words ▾

Inactive Ingredients sesame oil

🎯 Purpose 4 words ▾

Purpose Toothache relief agent

📄 When Using This Product 50 words ▾

When using this product use only in teeth with persistent, throbbing pain avoid touching tissues other than tooth cavity. Contact with lips or mucous membranes can cause burning, swelling, or irritation. DO NOT SWALLOW to avoid irritation do not use for more than 7 days do not exceed recommended dosage

📄 Stop Use and Ask a Doctor If 47 words ▾

Stop use and ask a dentist or doctor if irritation persists, inflammation develops, or if fever and infection develop See a dentist as soon as possible whether or not the pain is relieved. Toothaches and open cavities indicate serious problems that need prompt attention by a dentist.

📄 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.

📄 Questions or Comments 9 words ▾

Questions 1-877-636-2677 MON-FRI 9 AM to 5 PM (EST)

📄 Package Label / Principal Display Panel 20 words ▾

Package Label/Principal Display Panel Package Label Principal Display Panel Front

Package Label/Principal Display Panel Package Label Principal Display Panel Back

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 Red Cross Toothache (this brand).

Top reported reactions

Chemical Burn4
Hypersensitivity3
Fatigue2
Hypoaesthesia2
Swelling2
Abdominal Discomfort1
Aphthous Ulcer1

Age at onset

Adult1
Elderly1

Reporter sex

25 reports
Male · 29%
Female · 71%

Serious outcomes

Hospitalization2
Life-threatening2
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 5 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 The Mentholatum Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
The Mentholatum Company 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.
← 10742-0004-01 · The 10742-0020-01 · The →
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.