ABC Sore Throat Menthol Flavor

PHENOL ORAL HUMAN OTC DRUG

ABC Sore Throat Menthol Flavor is an FDA drug label for the active ingredient PHENOL manufactured by AMERISOURCE BERGEN administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260713.

Generic name
PHENOL
Manufacturer
AMERISOURCE BERGEN
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
46122-749
Application
M022
Label effective
20260713

About this product

ABC Sore Throat Menthol Flavor is an FDA-registered drug product whose active ingredient is PHENOL. It is labelled by AMERISOURCE BERGEN taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 46122-749, application M022, label effective 20260713. It is one of 9 FDA drug label records sharing the active ingredient PHENOL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing PHENOL are most often described in connection with: temporarily relieves, occasional minor, irritation pain, sore mouth. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Phenol 1.4%

Indications & Usage

Uses For the temporarily relieves of occasional minor irritation, pain, sore mouth, and sore throat.

Dosage & Administration

Directions ▪ Adults and children 12 year of age and older: Apply to 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 6 years to under 12 of age: Should be supervised in use of this product. ▪ Children under 6 years : Consult a doctor or dentist

Warnings

Warnings Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 6 years of age unless directed by doctor. When using this product, do not exceed recommended dosage. Stop use and ask a doctor or dentist if ▪ sore mouth 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. In case of overdose or accidental poisoning, get medical help or contact a Poison Control Center right away (1-800-222-1222).

More products with the same ingredient

PHENOL

CVS Health Sore Throat Fast Relief Oral Anesthetic

CVS Pharmacy,Inc. View label

CVS Sore Throat Cherry

CVS Pharmacy,Inc. View label

CVS Sore Throat Menthol Flavor

CVS PHARMACY,INC. View label

DRx Choice Sore Throat Menthol Flavor

RARITAN PHARMACEUTICALS INC View label

Good Neighbor Sore Throat Cherry Flavor

AMERISOURCE BERGEN View label

SORE THROAT

Raritan Pharmaceuticals Inc View label

Sore throat cherry

Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) View label

How products containing PHENOL compare

FDA lists 9 drug label records with PHENOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — AMERISOURCE BERGEN 2
— — CVS Pharmacy,Inc. 2
— — CVS PHARMACY,INC. 1
— — Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) 1
— — RARITAN PHARMACEUTICALS INC 1

Recall and safety notices

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-1066-2013 Ifosfamide Injection 3g/60 mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4496-22 AmeriSource Bergen Class II Terminated 20131009
D-1065-2013 Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22 AmeriSource Bergen Class II Terminated 20131009

Frequently asked questions

What is ABC Sore Throat Menthol Flavor used for?
Uses For the temporarily relieves of occasional minor irritation, pain, sore mouth, and sore throat.

Who makes ABC Sore Throat Menthol Flavor?
AMERISOURCE BERGEN is the labeler of record for ABC Sore Throat Menthol Flavor. 9 FDA label records share the active ingredient PHENOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does ABC Sore Throat Menthol Flavor come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is ABC Sore Throat Menthol Flavor prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing PHENOL?
Yes. 9 FDA drug label records list PHENOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has ABC Sore Throat Menthol Flavor been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.