La Vaquita New Extra
La Vaquita New Extra is an FDA drug label for the active ingredient METHYL SALICYLATE, MENTHOL manufactured by Delon Laboratories (1990) Ltd administered by TOPICAL. 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 20260901.
- Generic name
- METHYL SALICYLATE, MENTHOL
- Manufacturer
- Delon Laboratories (1990) Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 61734-301
- Application
- M017
- Label effective
- 20260901
About this product
La Vaquita New Extra is an FDA-registered drug product whose active ingredient is METHYL SALICYLATE, MENTHOL. It is labelled by Delon Laboratories (1990) Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 61734-301, application M017, label effective 20260901. It is one of 9 FDA drug label records sharing the active ingredient METHYL SALICYLATE, MENTHOL. 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 METHYL SALICYLATE, MENTHOL are most often described in connection with: temporary relief, minor aches, pains muscles. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses for the temporary relief of minor aches and pains of muscles and joints
Dosage & Administration
Directions adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: do not use, consult a doctor
Warnings
Warnings For external use only When using this product avoid contact with the eyes do not bandage tightly do not apply to wounds or damaged skin 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 If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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View labelHow products containing METHYL SALICYLATE, MENTHOL compare
FDA lists 9 drug label records with METHYL SALICYLATE, MENTHOL 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 form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Asclemed USA, Inc | 2 |
| — | — | STL International INC | 2 |
| — | — | Delon Laboratories (1990) Ltd | 1 |
| — | — | Human Science, LLC | 1 |
| — | — | Isagenix International, LLC | 1 |
Frequently asked questions
What is La Vaquita New Extra used for?
Uses for the temporary relief of minor aches and pains of muscles and joints
Who makes La Vaquita New Extra?
Delon Laboratories (1990) Ltd is the labeler of record for La Vaquita New Extra. 9 FDA label records share the active ingredient METHYL SALICYLATE, MENTHOL, 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 La Vaquita New Extra come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is La Vaquita New Extra 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 METHYL SALICYLATE, MENTHOL?
Yes. 9 FDA drug label records list METHYL SALICYLATE, MENTHOL 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 La Vaquita New Extra 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.
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.