Home › NDC Lookup › Ingredients › Camphor 10% › 49348-0148-30
Sunmark Camphor Spirit Camphor 10% 100 mg/mL Liquid, 59 mL — NDC 49348-0148-30 package photo

Sunmark Camphor Spirit Camphor 10% 100 mg/mL Liquid, 59 mL

by Strategic Sourcing Services LLC · 59 mL in 1 BOTTLE, PLASTIC (49348-148-30)
NDC 49348-0148-30
🏷️ FDA NDC (as labeled) 49348-148-30 billing pads the product 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) 49348-148-30
Product NDC 49348-148
11-digit billing NDC 49348014830
NCPDP billing unit ML — per mL (volume)
RxCUI 204935
UNII N20HL7Q941
UPC 0010939149336
Application # M017
SPL Set ID 667b3a9f-4a5c-4ef0-adbd-cce9a5f94faa
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-01-01
Route TOPICAL
Dosage form LIQUID
Substance CAMPHOR (NATURAL)
GPI-14 96200030109200
GPI class SM Camphor Spirit
GCN Seq No 006102
GCN 23890
HICL code 002617
Ingredient (HICL) Camphor
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L6
Therapeutic class — intermediate (HIC2) Irritants
HIC3 code L6A
Therapeutic class — specific (HIC3) Irritants/Counter-Irritants
AHFS code 84:92.00.00
AHFS class Skin And Mucous Membrane Agents, Misc.
FDB label name SM CAMPHOR SPIRIT
FDB brand name Camphor
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 49348-148-30 — 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 → 49348-0148-30. 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

LabelerStrategic Sourcing Services LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code49348
First marketedJan 2008
Product typeHuman Otc Drug
Portfolio316 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

Label name SM CAMPHOR SPIRIT Ingredient Camphor
🧪 What is this product?

Sunmark Camphor Spirit is a topical liquid containing 10% natural camphor, marketed as an over-the-counter monograph drug. Camphor is typically used in topical products for its warming or cooling sensations on the skin. This product is applied directly to the skin surface and is commonly found in remedies intended to provide localized comfort, though individual results vary.

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.

🧪 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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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.

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

The official label also statesAlcohol 84%, 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.

💲 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 $0.045 $2.64 / 59 ml
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 mL) — tap or hover for the price & month
Sep 2023 Jan 2025 $0.045 $0.043
▲ Up 3% over the last 2 months.
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
Sunmark Camphor Spirit 100 mg/mLthis 49348-0148-30 Strategic 59 ml $0.045 — FDA listed —
LEADER Camphor Spirit 100 mg/mL 70000-0396-01 Cardinal 59 ml $0.048 — Availability likely +8%
Camphor Spirit 100 mg/mL 70677-1201-01 Strategic 59 ml $0.048 — Availability likely +8%
HUMCO Camphor Spirit 100 mg/mL 00395-0467-16 Humco 473 ml — — FDA listed —
DDM Camphor Spirit 100 mg/mL 53943-0467-92 Discount 59 ml — — FDA listed —
Quality Choice Camphor Spirit 100 mg/mL 63868-0490-02 Chain 473 ml — — FDA listed —
Camphor Spirit 100 mg/mL 82645-0920-92 Pharma 59 ml — — 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

🏛️
2008
On the market since
Jan 2008
📍
2026
Currently FDA-listed
18 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.

🔬 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 Camphor 10% — the ingredient across all brands.

Top reported reactions

Somnolence1

Reporter sex

1 reports
Female · 100%
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
49348-0148-30 You're viewing this 59 mL in 1 BOTTLE, PLASTIC (49348-148-30) 2017-12-12 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 20 words ▾

Use For the temporary relief of minor aches, muscle and joint pain associated with arthritis, strains, brusies and simple backache.

⏱️ Dosage and Administration 40 words ▾

Directions (dilute 3 parts olive oil and mix well) Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily. Children under 2 yrs of age: consult a doctor befre use.

⚠️ Warnings 57 words ▾

Warnings For external use only. Do not drink. If swallowed, immediately give 3 or 4 glases of water. Do not induce vomiting. If vomiting occurs, give fluids again. Do not give anything by mouth to an unconscious or convulsing person. Get medical attention immediately. Avoid contact with eyes or mucous membranes. Do not apply to irritated skin.

🧪 Active Ingredient 4 words ▾

Active Ingredient Camphor 10%

🧪 Inactive Ingredients 6 words ▾

Inactive ingredients Alcohol 84%, Purified Water

🎯 Purpose 2 words ▾

Purpose Counterirritant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 49348-0138-30 · Strategic 49348-0149-29 · Strategic →
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.