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Campho-Phenique Antiseptic CAMPHOR (SYNTHETIC) and PHENOL 10.8 mg/100mL; 4.7 mg/100mL Liquid — NDC 69536-110-75 (Billing 69536-0110-75)

by Foundation Consumer Healthcare LLC · 1 BOTTLE in 1 CARTON / 22 mL in 1 BOTTLE

This is a package of Campho-Phenique Antiseptic CAMPHOR (SYNTHETIC) and PHENOL 10.8 mg/100mL; 4.7 mg/100mL Liquid from Foundation Consumer Healthcare LLC, marketed since Jun 2017 and currently FDA-listed. It is this product's only package size.

NDC 69536-0110-75
🏷️ FDA NDC (as labeled) 69536-110-75 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69536-110-75
Product NDC 69536-110
11-digit billing NDC 69536011075
NCPDP billing unit ML — per mL (volume)
RxCUI 210346, 308940
UNII 5TJD82A1ET, 339NCG44TV
Application # M017
SPL Set ID 82edaef0-0709-4ae1-a664-c9c5adb91ee1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-06-01
Route TOPICAL
Dosage form LIQUID
Substance CAMPHOR (SYNTHETIC); PHENOL
Quick answers
  • RxCUI (RxNorm): 210346
Why two NDCs? The FDA registers this code as 69536-110-75 — 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 → 69536-0110-75. 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?

Campho-Phenique Antiseptic is a topical liquid containing camphor and phenol. Both ingredients are commonly used in over-the-counter products for their numbing and antimicrobial properties on minor skin irritations. This product is marketed as an OTC monograph drug, meaning it is manufactured according to FDA's established guidelines for antiseptic products rather than as an individually approved application. It is applied directly to the skin.

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
69536-0110-75 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 22 mL in 1 BOTTLE 2021-11-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
HEB Camphor Phenol 108 mg/mL; 47 mg/mL 37808-0105-05 H 45 ml — — FDA listed —
DDM Instant Antiseptic Pain Relief 108 mg/mL; 47 mg/mL 53943-0105-05 Discount 45 ml — — FDA listed —
Instant Antiseptic Pain Relief 108 mg/mL; 47 mg/mL 63868-0060-45 Chain 45 ml — — FDA listed —
Premier Value Instant Antiseptic Pain Relief 108 mg/mL; 47 mg/mL 68016-0821-45 Pharmacy 45 ml — — FDA listed —
Campho-Phenique Antiseptic 10.8 mg/100mL; 4.7 mg/100mLthis 69536-0110-75 Foundation 1 bottle — — FDA listed —
Antiseptic Instant Pain Relief 108 mg/mL; 47 mg/mL 82645-0902-05 Pharma 45 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

🏛️
2017
On the market since
Jun 2017
📍
2026
Currently FDA-listed
9 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerFoundation Consumer Healthcare LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code69536
First marketedJun 2017
Product typeHuman Otc Drug
Portfolio9 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 📦 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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

Uses for temporary relief of pain and itching associated with insect bites minor burns sunburn minor cuts scrapes cold sores first aid to help protect against infection in minor cuts scrapes burns

⏱️ Dosage and Administration 41 words ▾

Directions adults and children 2 years of age and over: clean the affected area apply a small amount of this product on the area 1 to 3 times daily do not bandage children under 2 years of age: ask a doctor

⚠️ Warnings 116 words ▾

Warnings For external use only Do not use over large areas of the body with a bandage Ask a doctor before use if you have a deep or puncture wound animal bites serious burns When using this product do not use in or near the eyes. If contact occurs, rinse eyes thoroughly with water and obtain medical attention. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. Do not induce vomiting before contacting medical help or a Poison Control Center.

📦 Storage and Handling 17 words ▾

Other information store at room temperature. Avoid excessive heat above 40°C (104°F). close cap tightly after use

🧪 Active Ingredient 9 words ▾

Active ingredient Camphorated phenol (camphor 10.8% and phenol 4.7%)

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients light mineral oil, aloe barbadensis leaf extract, eucalyptus oil

🎯 Purpose 3 words ▾

Purposes Pain reliever/antiseptic

📄 Do Not Use 12 words ▾

Do not use over large areas of the body with a bandage

📄 Ask a Doctor Before Use If 17 words ▾

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

📄 When Using This Product 24 words ▾

When using this product do not use in or near the eyes. If contact occurs, rinse eyes thoroughly with water and obtain medical attention.

📄 Stop Use and Ask a Doctor If 26 words ▾

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

📄 Keep Out of Reach of Children 32 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not induce vomiting before contacting medical help or a Poison Control Center.

📄 Questions or Comments 11 words ▾

Questions or comments? 1-855-602-2676 weekdays 9 AM to 5 PM EST

📄 Package Label / Principal Display Panel 48 words ▾

PRINCIPAL DISPLAY PANEL - 22 mL Bottle Carton with aloe MAXIMUM STRENGTH MEDICATED CAMPHO PHENIQUE ® PAIN & ITCH RELIEF ANTISEPTIC LIQUID Multi-purpose formula insect bites minor burns cuts, scrapes & irritations Helps prevent infection 3/4 FL OZ (22 mL) Principal Display Panel - 22 mL Bottle Carton

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Foundation Consumer Healthcare LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Foundation Consumer Healthcare 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.
← 69536-0109-50 · Foundation 69536-0133-88 · Foundation →
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.