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Absorbine Jr. Plus Menthol 4 g/100mL Liquid — NDC 69693-411-04 (Billing 69693-0411-04)

by Clarion Brands, LLC · 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 118 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of Absorbine Jr. Plus Menthol 4 g/100mL Liquid from Clarion Brands, LLC, marketed since Jun 2010 and currently FDA-listed. It is this product's only package size.

NDC 69693-0411-04
🏷️ FDA NDC (as labeled) 69693-411-04 billing pads the product 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

⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69693-411-04
Product NDC 69693-411
11-digit billing NDC 69693041104
RxCUI 283438, 751892
UNII L7T10EIP3A
Application # M017
SPL Set ID fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-06-24
Route TOPICAL
Dosage form LIQUID
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 283438
Why two NDCs? The FDA registers this code as 69693-411-04 — 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 → 69693-0411-04. 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

📗 Our plain-language guide HelloPharmacist
  • Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
  • It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
  • A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
  • No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
📖 Read our full Menthol guide →

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
69693-0411-04 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 118 mL in 1 BOTTLE, WITH APPLICATOR 2010-06-24 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
blue goo FREEZING PAIN RELIEF Topical Analgesic 40 mg/mL 67385-0286-01 Garcoa, 74 ml — — FDA listed —
Absorbine Jr. Plus 4 g/100mLthis 69693-0411-04 Clarion 1 bottle — — FDA listed —
Absorbine Jr. Plus 4 g/100mL 69693-0424-04 Clarion 1 bottle — — FDA listed —
AUVON Pain Relief Roll-on 4 g/100mL 83391-0003-01 SHENZHEN 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

🏛️
2010
On the market since
Jun 2010
📍
2026
Currently FDA-listed
16 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 1364PS73AF
    Acetone is a clear, volatile liquid solvent. In medications, it helps dissolve or extract active ingredients during manufacturing and may be used in certain liquid formulations or coating processes.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 4N9P6CC1DX
    A plant extract from echinacea species, commonly used in herbal formulations. It may serve as a flavoring agent, botanical ingredient, or contribute to the product's intended herbal profile in supplements or botanical medicines.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII 9679TC07X4
    Iodine is a chemical element used in medicines as an antiseptic and preservative. It helps prevent bacterial and fungal growth, keeping the product safe and stable during storage.
  • UNII 1C4QK22F9J
    Potassium iodide is an inorganic salt that supplies iodine. In medicines, it acts as a preservative and stabilizer to prevent degradation of active ingredients and extend shelf life.
  • UNII 3J50XA376E
    Thymol is a natural compound derived from thyme and other plants. It acts as a preservative and flavoring agent in medicines, helping prevent microbial growth and add taste.
  • 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.
  • UNII F84709P2XV
    Wormwood is a plant extract used as a flavoring agent in medicines. It provides a bitter taste to help mask other flavors or make the medication easier to take.
  • UNII 01756N87N8
    Wormwood oil is a volatile oil extracted from the wormwood plant. It's used in medicines as a flavoring agent and fragrance to improve taste and smell.

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

The official label also statesacetone, chloroxylene, FD&C blue #1, Iodine, plant extracts of calendula, echinacea, wormwood herb, potassium iodide, thymol, water, and wormwood 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

LabelerClarion Brands, LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code69693
First marketedJun 2010
Product typeHuman Otc Drug
Portfolio25 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 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 21 words ▾

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

⏱️ Dosage and Administration 32 words ▾

Directions adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily children under 2 years of age; consult a doctor

⚠️ Warnings 22 words ▾

Warnings For external use only. Use only as directed. Flammable Keep away from fire, flame, sparks and heated surfaces. Tighten cap firmly.

🧪 Active Ingredient 4 words ▾

Active Ingredient Menthol 4.0%

🧪 Inactive Ingredients 22 words ▾

Inactive Ingredients acetone, chloroxylene, FD&C blue #1, Iodine, plant extracts of calendula, echinacea, wormwood herb, potassium iodide, thymol, water, and wormwood oil

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 When Using This Product 21 words ▾

When using this product Avoid contact with the eyes Do not apply to wounds or damaged skin Do not bandage tightly

📄 Stop Use and Ask a Doctor If 27 words ▾

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

🤰 If Pregnant or Breast-Feeding 11 words ▾

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

📄 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 3 words ▾

Questions? Call 1-844-922-7672

📄 Package Label / Principal Display Panel ~1 min read ▾

Principal Display Panel Extra Strength Formula ABSORBINE jr. ® PLUS Pain Relieving Liquid Fast Absorbing for Rapid Relief Relieves: • Sore Muscles • Arthritis Pain No Mess Applicator Keeps Hands Clean 4 FL OZ (118 ml) Our fast absorbing, deep penetrating Extra Strength Formula provides even more relief to sore muscles, arthritis pain & stiffness Fast relief from; • Sore Muscles & Cramps • Aching Joints & Stiffness • Arthritis Pain • Bruises • Sprains • Strains • Backache • Foot Pain & Discomfort Our Extra Strength Formula is: • Fast acting • Easy to apply • Quick-drying • Non-greasy • Non-stinging MADE WITH PRIDE IN THE U.S.A.

Distributed by: Clarion Brands, LLC 27070 Miles Rd., Suite A Solon, OH 44139 1-844-922-7672 88749A www.absorbinejr.com Extra Strength ABSORBINE ® jr. QUALITY RELIEF SINCE 1903 4% MENTHOL Pain Relieving Liquid Fast Absorbing for Rapid Relief • Sore Muscles • Aching Joints • Arthritis Pain 4 FL OZ (118 ml) Make Pain History. Absorbine Jr. has been making aches, pains, arthritis, and sore muscles a thing of the past for over 120 years.

Our non-greasy formula, with an easy-to-apply applicator, penetrates deep and goes to work instantly for fast acting pain relief. • TARGETED PAIN RELIEF • FAST ACTING • NO MESS LIQUID APPLICATOR Distributed by: Absorbine Jr. LLC 811 Broad Street, Suite 600 Chattanooga, TN 37402 @2023 www.absorbinejr.com 1000153 Absorbine Jr. Plus Carton Absorbine Jr.

Plus Label

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 Absorbine Jr. Plus (this brand).

Top reported reactions

Dyspnoea86
Fatigue84
Pain83
Pruritus78
Headache68
Dizziness67
Cough65

Age at onset

Infant1
Child1
Adolescent1
Adult97
Elderly90

Reporter sex

1,005 reports
Male · 38%
Female · 62%
Unknown · 0%

Serious outcomes

Hospitalization338
Death125
Life-threatening46
Disabling26
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 97 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 — Not published for this NDC No photo available yet for this listing.
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 Clarion Brands, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Clarion Brands, 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.
← 69693-0108-25 · Clarion 69693-0412-01 · Clarion →
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.