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S.T.37 Hexylresorcinol 1.1 mg/mL Solution — NDC 69846-0860-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

S.T.37 Hexylresorcinol 1.1 mg/mL Solution — NDC 69846-860-01 (Billing 69846-0860-01)

by NUMARK BRANDS, INC · 1 BOTTLE in 1 CARTON / 473 mL in 1 BOTTLE

This is a package of S.T.37 Hexylresorcinol 1.1 mg/mL Solution from NUMARK BRANDS, INC, marketed since Nov 1929 and currently FDA-listed.

NDC 69846-0860-01
🏷️ FDA NDC (as labeled) 69846-860-01 billing pads the product segment with a zero
This package
Contains473 mL in 1 bottle Pack sizes2 compare ↓
Product page 69846-0860-00 Also comes in: 236.5 mL 69846-860-00
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69846-860-01
Product NDC 69846-860
11-digit billing NDC 69846086001
UNII R9QTB5E82N
Application # M022
SPL Set ID 7d7acca2-aa8a-5272-e813-faab039cc798
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1929-11-20
Route ORAL, TOPICAL
Dosage form SOLUTION
Substance HEXYLRESORCINOL
Why two NDCs? The FDA registers this code as 69846-860-01 — 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 → 69846-0860-01. 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

🧪 What is this product?

S.T.37 is an over-the-counter oral and topical solution containing hexylresorcinol, an antimicrobial and antiseptic ingredient. When taken by mouth or applied to the skin or mouth tissues, hexylresorcinol is typically used to help reduce bacteria and promote cleansing of minor wounds, sore throats, and oral irritation. This product is marketed under the FDA's over-the-counter monograph rules for antiseptic and antimicrobial agents.

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.
Try another pack size: 236.5 mL
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
69846-0860-00 69846-860-00 Main listing 1 BOTTLE in 1 AMPULE / 236.5 mL in 1 BOTTLE 1929-11-20 — Active
69846-0860-01 You're viewing this 1 BOTTLE in 1 CARTON / 473 mL in 1 BOTTLE 1929-11-20 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle in 1 carton / 473 ml in 1 bottle.
What NDC number is used to bill for this package of S.T.37 Hexylresorcinol 1.1 mg/mL Solution?
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
S.t.37 1.1 mg/mLthis 69846-0860-01 NUMARK 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

🏛️
1929
On the market since
Nov 1929
📍
2026
Currently FDA-listed
97 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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 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 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 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII TZX5469Z6I
    Sodium bisulfite is a chemical salt used as a preservative and antioxidant in medicines. It prevents discoloration and degradation of active ingredients, especially in liquid formulations and injectables.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • 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.

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

The official label also statescitric acid, edetate disodium, glycerin, propylene glycol, sodium bisulfite, sodium citrate, purified 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.

Manufacturer & labeler

LabelerNUMARK BRANDS, INC
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code69846
First marketedNov 1929
Product typeHuman Otc Drug
Portfolio4 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.

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 and Cautions ⚠️ Warnings 📦 Storage and Handling 🧪 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 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Uses temporarily relieves: minor irritations of the mouth minor pain in the mouth sore mouth sore throat first aid to help prevent skin infection in minor cuts, scrapes, and burns

⏱️ Dosage and Administration 97 words ▾

Directions (as a First Aid antiseptic) use full strength clean affected area apply a small amount of product on the area use 1-3 times daily may be covered with a sterile bandage if bandaged let dry first

Directions (as an Oral pain reliever) apply to affected area gargle, swish around, or allow to remain in place for at least one minute and then spit out adults and children 2 years old and over use up to 4 times daily or as directed by a dentist or doctor children under 2 years old ask a dentist or doctor

⚠️ Warnings and Cautions 30 words ▾

Sore throat warning if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly.

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 13 words ▾

Other Information store at controlled room temperature 59° - 86°F (15° - 30°C)

🧪 Active Ingredient 11 words ▾

Active Ingredient Purposes Hexylresorinol 0.1% Oral Pain Reliever First aid antiseptic

🧪 Inactive Ingredients 15 words ▾

Inactive Ingredients citric acid, edetate disodium, glycerin, propylene glycol, sodium bisulfite, sodium citrate, purified water.

🎯 Purpose 11 words ▾

Active Ingredient Purposes Hexylresorinol 0.1% Oral Pain Reliever First aid antiseptic

📄 Do Not Use 12 words ▾

Do not use In the eyes over large areas of the body

📄 Ask a Doctor Before Use If 16 words ▾

Ask a doctor before use if you have deep or puncture wounds animal bites serious burns

📄 When Using This Product 9 words ▾

When using this product do not exceed recommended dosage

📄 Stop Use and Ask a Doctor If 45 words ▾

Stop use and ask a doctor if condition persists condition worsens you need to use product longer than 1 week

Stop use and ask a doctor or dentist if sore mouth symptoms do not improve in 7 days irritation, pain, and redness persist or worsen

🤰 If Pregnant or Breast-Feeding 11 words ▾

If pregnant or breast feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 3 words ▾

Questions call 1-800-214-2379

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL 8 oz SIZE 2.5 more ounces at the same low price S.T.37 ® FIRST AID ANTISEPTIC/ORAL PAIN RELIEVER SOLUTION FOR BURNS, CUTS, ABRASIONS & HYGIENIC CARE OF THE MOUTH. Do not use if foil seal under cap is broken or missing at time of purchase 8 FL OZ (236.5 mL) WON'T STING — WON'T STAIN S.T.37 kills common pathogenic bacteria quickly — on contact! Laboratory tests have established S.T.37 antiseptic solution as a general antiseptic for household use.

S.T.37 is pleasant to use because it produces little or no stinging or burning. In fact, it soothes irritated areas. S.T.37 does not stain the skin or leave an order.

Everyday Uses for S.T.37 Cuts & Abrasions: Apply full strength S.T.37 into the cut or over the injured area. Since it is germicidal for the common pathogenic bacteria, S.T.37 may minimize the development of infection. Excellent for cleansing cuts and scrapes.

Burns: Apply full strength S.T.37 for treatment of minor burns. S.T.37 combats the cause of infections. Hygienic Care of Mouth: Use undiluted and gargle or rinse to help keep mouth clean and fresh.

S.T.37 temporarily relieves minor pain and protects irritated areas of a sore mouth or throat. Distributed by Numark Brands, Inc. 27070 Miles Rd, Suite A, Solon Ohio 44139 www.numarkbrands.com B10082 Rev.

3/18 S.T.37 ® FIRST AID ANTISEPTIC/ORAL PAIN RELIEVER SOLUTION FOR BURNS, CUTS, ABRASIONS & HYGIENIC CARE OF THE MOUTH 8 FL OZ (236.5 mL) Do not use if foil seal under cap is broken or missing at time of purchase S.T.37 kills common pathogenic bacteria quickly - on contact! Laboratory tests have established S.T.37 antiseptic solution as a general antiseptic for household use. S.T.37 is pleasant to use because it produces little or no stinging or burning.

In fact, it soothes irritated areas. S.T.37 does not stain the skin or leave an order. Everyday Uses for S.T.37 Cuts & Abrasions: Apply full strength S.T.37 into the cut or over the injured area.

Since it is germicidal for the common pathogenic bacteria, S.T.37 may minimize the development of infection. Excellent for cleansing cuts and scrapes. Burns: Apply full strength S.T.37 for treatment of minor burns.

S.T.37 combats the cause of infections. Hygienic Care of Mouth: Use undiluted and gargle or rinse to help keep mouth clean and fresh. S.T.37 temporarily relieves minor pain and protects irritated areas of a sore mouth or throat.

Distributed by Numark Brands, Inc. 27070 Miles Rd, Suite A, Solon Ohio 44139 1-800-214-2379 www.numarkbrands.com Rev. 3/18 J12008

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 S.T.37 (this brand).

Top reported reactions

Rash3
Hepatic Function Abnormal2
Bowel Movement Irregularity1
Bronchopulmonary Aspergillosis1
Constipation1
Cytokine Release Syndrome1
Diarrhoea1

Age at onset

Elderly2

Reporter sex

12 reports
Male · 55%
Female · 45%

Serious outcomes

Hospitalization3
Death2
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 4 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 NUMARK BRANDS, INC. 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 1 other package presentation of this same product, including 1 bottle (69846-0860-00). 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?
NUMARK BRANDS, INC 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.
← 69846-0110-42 · NUMARK 69846-0911-61 · NUMARK →
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.