Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
PHENOL 14 mg/100mL Spray, 177 mL — NDC 83324-031-06 (Billing 83324-0031-06)
by CHAIN DRUG MARKETING ASSOCIATION INC. · 177 mL in 1 BOTTLE, SPRAY
This is a package of 177 mL of PHENOL 14 mg/100mL Spray from CHAIN DRUG MARKETING ASSOCIATION INC., marketed since Dec 2024 and currently FDA-listed. It is this product's only package size.
NDC 83324-0031-06
🏷️ FDA NDC (as labeled)
83324-031-06
billing pads the product segment with a zero
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
83324-031-06
Product NDC
83324-031
11-digit billing NDC
83324003106
UNII
339NCG44TV
UPC
0635515975361
Application #
M022
SPL Set ID
2379e23a-72fe-4e94-9d7e-9b623c0db174
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-12-12
Route
NASAL
Dosage form
SPRAY
Substance
PHENOL
Why two NDCs?
The FDA registers this code as 83324-031-06 — 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 → 83324-0031-06. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
📗 Our plain-language guide HelloPharmacist
- Phenol is an anesthetic and antiseptic ingredient, meaning it temporarily numbs the area where you apply it and may help reduce minor surface irritation. It's designed to give you...
- What is phenol actually doing when I spray it on my sore throat?
- For products like Chloraseptic sprays, you should hold it in place for at least 15 seconds before spitting it out — that gives the ingredient time to work on the affected area. You...
- How long should I hold the spray in my mouth before spitting it out?
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Phenolphthalein — tap one for details:
3
Nutrient depletion considerations
Phenolphthalein may be associated with lower levels of 3 nutrients — worth a chat with your pharmacist, not a cause for alarm.
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about PHENOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per mL | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 83324-0031-06 You're viewing this Main listing | 177 mL in 1 BOTTLE, SPRAY | 2024-12-12 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Sore Throat Cherry 1.4 g/100mL 63868-0811-55 | QUALITY | 177 ml | $0.011 | — | FDA listed | — |
| Rugby Cherry Flavor 1.4 g/100mL 00536-1228-58 | RUGBY | 177 ml | $0.012 | — | Availability likely | — |
| Sore Throat Cherry 1.5 g/100mL 00904-6305-21 | Major | 177 ml | $0.012 | — | Availability likely | — |
| Good Neighbor Sore Throat Cherry Flavor 1.4 g/100mL 46122-0748-76 | AMERISOURCE | 177 ml | $0.012 | — | Availability likely | — |
| ABC Sore Throat Menthol Flavor 1.4 g/100mL 46122-0749-76 | AMERISOURCE | 177 ml | $0.012 | — | Availability likely | — |
| Sore Throat Relief Cherry Flavor 1.4 g/100mL 70000-0458-01 | Cardinal | 177 ml | $0.012 | — | Availability likely | — |
| QUALITY CHOICE Sore Throat 1.4 g/100mL 83324-0275-06 | CHAIN | 177 ml | $0.012 | — | Availability likely | — |
| Sore throat cherry 1.4 g/100mL 00363-0376-06 | Walgreens | 177 ml | — | — | FDA listed | — |
| Walgreens Sore Throat Cherry Flavor 1.4 g/100mL 00363-7030-06 | WALGREEN | 177 ml | — | — | FDA listed | — |
| Sore Throat 1.4 g/100mL 11822-3109-08 | Rite | 177 ml | — | — | FDA listed | — |
| Signature Care Sore Throat Cherry Flavor 1.4 g/100mL 21130-0196-06 | SAFEWAY | 177 ml | — | — | FDA listed | — |
| Sore Throat 1.4 g/100mL 21130-0376-06 | Safeway, | 177 ml | — | — | FDA listed | — |
| TopCare Cherry Flavor 1.4 g/100mL 36800-0600-06 | TOPCO | 177 ml | — | — | FDA listed | — |
| Topcare Sore Throat Menthol Flavor 1.4 g/100mL 36800-0606-06 | TOPCO | 177 ml | — | — | FDA listed | — |
| HEB Sore Throat Cherry Flavor 1.4 g/100mL 37808-0803-06 | HEB | 177 ml | — | — | FDA listed | — |
| HEB Sore Throat Menthol Flavor 1.4 g/100mL 37808-0805-06 | HEB | 177 ml | — | — | FDA listed | — |
| PUBLIX Sore Throat Menthol Flavor 1.4 g/100mL 41415-0307-06 | PUBLIX | 177 ml | — | — | FDA listed | — |
| PUBLIX Sore Throat Fast Relief Oral Anesthetic 1.4 g/100mL 41415-0703-06 | PUBLIX | 177 ml | — | — | FDA listed | — |
| Sore Throat 1.4 g/100mL 49035-0376-06 | EQUATE | 177 ml | — | — | FDA listed | — |
| Sore Throat ReadyInCase 1.4 g/100mL 49580-0376-06 | P | 177 ml | — | — | FDA listed | — |
| CVS Sore Throat Cherry 1.4 g/100mL 51316-0306-06 | CVS | 177 ml | — | — | FDA listed | — |
| CVS Sore Throat Menthol Flavor 1.4 g/100mL 51316-0307-06 | CVS | 177 ml | — | — | FDA listed | — |
| Sore Throat Cherry 1.4 g/100mL 55319-0376-06 | Family | 177 ml | — | — | FDA listed | — |
| Sore throat cherry 1.4 g/100mL 55910-0376-06 | Dolgencorp, | 177 ml | — | — | FDA listed | — |
| Sore Throat Menthol 1.4 g/100mL 56062-0377-06 | Publix | 177 ml | — | — | Discontinued | — |
| CVS Health Sore Throat Fast Relief Oral Anesthetic 1.4 g/100mL 59779-0895-06 | CVS | 177 ml | — | — | FDA listed | — |
| Diabetic Tussin Sore Throat Cherry 1.4 mg/mL 61787-0066-06 | MEDTECH | 177 ml | — | — | FDA listed | — |
| Sore Throat Relief Cherry 1.4 g/100mL 63941-0376-06 | Best | 177 ml | — | — | FDA listed | — |
| Sore Throat Relief 1.4 g/100mL 67091-0267-17 | WinCo | 177 ml | — | — | FDA listed | — |
| Chloraseptic Childrens Sore Throat Cherry 1.4 g/100mL 67172-0930-06 | Prestige | 177 ml | — | — | FDA listed | — |
| Sore Throat Relief Cherry Flavor 1.4 g/100mL 68016-0342-06 | Chain | 177 ml | — | — | FDA listed | — |
| Sore Throat Relief Menthol 1.4 g/100mL 68016-0343-06 | Chain | 177 ml | — | — | FDA listed | — |
| DRx Choice Sore Throat Menthol Flavor 1.4 g/100mL 68163-0307-06 | RARITAN | 177 ml | — | — | FDA listed | — |
| Sore Throat 1.4 g/100mL 68163-0703-06 | Raritan | 177 ml | — | — | FDA listed | — |
| NICE SORE THROAT Cherry 1.4 g/100mL 69626-0047-06 | Leosons | 177 ml | — | — | FDA listed | — |
| Phenol 14 mg/100mLthis 83324-0031-06 | CHAIN | 177 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2024
On the market since
Dec 2024
📍
2026
Currently FDA-listed
2 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.
- FDA Orange Book · refreshed Sep 3, 2026
What it looks like
FlavorCherry
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
- FDA label on DailyMed · label index refreshed Oct 1, 2026
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 WZB9127XOA
A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
-
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 SB8ZUX40TY
Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter 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.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statescherry flavor, FD&C Red #40, glycerin, purified water, sodium saccharin.
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerCHAIN DRUG MARKETING ASSOCIATION INC.
FDA applicationM022 (OTC MONOGRAPH DRUG)
Labeler code83324
First marketedDec 2024
Product typeHuman Otc Drug
Portfolio72 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 openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses For temporary relief of occasional minor throat irritation, pain, sore mouth, sore throat.
⏱️ Dosage and Administration ▾
Directions Adults and children 3 years of age and older. Apply to the affected area (one spray) Allow to remain in place for at least 15 seconds, then spit out Use every 2 hours or as directed by a doctor or dentist. Children under 12 years of age should be supervised in the use of this product.
Children under 3 years of age , consult a doctor or dentist Before using the first time, remove the protective neck band and dust cap from the tip. To spray hold bottle straight up and press the nozzle with index finger without tilting head. Fully depress pump all the way down with a firm, even stroke.
Wipe nozzle dry.
⚠️ Warnings ▾
Warnings Sore throat waring: Severe and persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a doctor. Whan using this product do not exceed recommended dose. Do not use more than 2 days. Use only as directed. Use of this container by more than one person may spread infection.
📦 Storage and Handling ▾
Other information Store at room temperature
🧪 Active Ingredient ▾
Active Ingredient Purpose Phenol 1.4%............. Oral Anesthetic/Analgesic
🧪 Inactive Ingredients ▾
Inactive ingredients cherry flavor, FD&C Red #40, glycerin, purified water, sodium saccharin.
🎯 Purpose ▾
Sore Throat Relief
📄 When Using This Product ▾
Sore throat waring: Severe and persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a doctor. Whan using this product do not exceed recommended dose. Do not use more than 2 days. Use only as directed. Use of this container by more than one person may spread infection.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor or dentist if sore throat symptoms do not improve in 7 days irritation, pain or redness persists or worsens swelling, rash or fever develops If pregnant or breast-feeding ask a doctor before use.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. In case of overdose or accidental poisoning, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL NDC-83324- 031 -06 containerlabel
No label section mentions that — try another word, or open the full label on DailyMed below.
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 PHENOL — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 CHAIN DRUG MARKETING ASSOCIATION INC.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
CHAIN DRUG MARKETING ASSOCIATION 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.
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.