Antiseptic Mouthrinse

Antiseptic Mouthrinse is an FDA-registered drug product whose active ingredient is EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL. It is labelled by Rockland Cosmetics, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 69892-072, application 505G(a)(3), label effective 20260520. 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.

Across FDA labelling, products containing EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL are most often described in connection with: helps control, leads gingivitis. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use helps control plaque that leads to gingivitis

Directions adults and children 12 years of age and older - vigorously swish 20 ml (2/3 FL OZ or 4 teaspoonfuls) between teeth twice a day for 30 seconds then spit out; do not swallow children under 12 years of age - consult a dentist or doctor this rinse is not intended to replace brushing or flossing

Warnings For this product

Adverse reaction Distributed By: Rockland Cosmetics, Inc. Hillburn, NY 10931 www.RocklandCosmetics.com Made in the U.S.A. with U.S. and foreign components. NSK New Square Kashrus DSP-TN-21091 DSP-MO-20087

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.

What is Antiseptic Mouthrinse used for?
Use helps control plaque that leads to gingivitis

Who makes Antiseptic Mouthrinse?
Rockland Cosmetics, Inc. is the labeler of record for Antiseptic Mouthrinse. 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 Mouthrinse 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 Mouthrinse 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 Mouthrinse been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

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.