Antiseptic

EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL ORAL HUMAN OTC DRUG

Antiseptic is an FDA drug label for the active ingredient EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL manufactured by WALMART INC. (see also Equate) 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 20260911.

Generic name
EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
Manufacturer
WALMART INC. (see also Equate)
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
79903-152
Application
M022
Label effective
20260911

About this product

Antiseptic is an FDA-registered drug product whose active ingredient is EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL. It is labelled by WALMART INC. (see also Equate) taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 79903-152, application M022, label effective 20260911. It is one of 23 FDA drug label records sharing the active ingredient EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL. 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 EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL are most often described in connection with: helps prevent, reduce plaque. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Eucalyptol (0.092%) Menthol (0.042%) Methyl Salicylate (0.060%) Thymol (0.064%)

Indications & Usage

Uses helps prevent and reduce plaque gingivitis

Dosage & Administration

Directions adults and children 12 years of age and older: vigorously swish 20 milliliters of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse. children 6 years to under 12 years of age: supervise use children under 6 years of age: do not use

Warnings

Warning Do not use in children under 12 years of age. Stop use and ask a dentist gingivitis, bleeding, or redness persists for more than 2 weeks you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease. Keep out of reach of children under 6 years of age If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

More products with the same ingredient

EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL

Antiseptic Mouth Rinse

The Kroger Co. View label

Antiseptic Mouth Rinse

Nice-Pak Products, LLC View label

Antiseptic Mouth Rinse

Nice-Pak Products, LLC View label

How products containing EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL compare

FDA lists 23 drug label records with EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL 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
— — Nice-Pak Products, LLC 4
— — Publix Super Markets, Inc. 3
— — WALMART INC. (see also Equate) 3
— — DISCOUNT DRUG MART 2
— — H E B 2

Recall and safety notices

5 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-0699-2026 Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670, Blaine Labs Inc Class II Ongoing 20260708
D-0627-2026 Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1. Elevate Oral Care Class II Ongoing 20260701
D-0361-2026 First Aid Only BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%), 5x7, bulk, Acme United Corporation, 2280 Tanner Road, Rocky Mount, NC, 27801 Made in USA, NDC 0924-7116-00. ACME UNITED CORPORATION Class II Ongoing 20260311
D-0366-2026 Med Nap BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 Towelettes, Manufactured by: Acme United Corporation, 1 Waterview Dr, Shelton, CT 06481, NDC 0924-0246-01. ACME UNITED CORPORATION Class II Ongoing 20260311
D-0376-2026 Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 5x7, 1000 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-04. ACME UNITED CORPORATION Class II Ongoing 20260311

Frequently asked questions

What is Antiseptic used for?
Uses helps prevent and reduce plaque gingivitis

Who makes Antiseptic?
WALMART INC. (see also Equate) is the labeler of record for Antiseptic. 23 FDA label records share the active ingredient EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL, 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 Antiseptic 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 Antiseptic 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 EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL?
Yes. 23 FDA drug label records list EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL 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 Antiseptic been recalled?
5 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.