MOSQUITO BUG OFF

DIETHYLTOLUAMIDE TOPICAL HUMAN OTC DRUG

MOSQUITO BUG OFF is an FDA drug label for the active ingredient DIETHYLTOLUAMIDE manufactured by Lydia Co., 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 20210628.

Generic name
DIETHYLTOLUAMIDE
Manufacturer
Lydia Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
72988-0005
Application
N/A
Label effective
20210628

About this product

MOSQUITO BUG OFF is an FDA-registered drug product whose active ingredient is DIETHYLTOLUAMIDE. It is labelled by Lydia Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72988-0005, label effective 20210628. 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 DIETHYLTOLUAMIDE are most often described in connection with: skin clothes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

DIETHYLTOLUAMIDE

Indications & Usage

You can spray it on your skin or clothes.

Dosage & Administration

for external use only

Warnings

do not use for the following people: infants under six months do not use excessive amounts or for long periods of time beyond the required do not use it in an enclosed area

Frequently asked questions

What is MOSQUITO BUG OFF used for?
You can spray it on your skin or clothes.

Who makes MOSQUITO BUG OFF?
Lydia Co., Ltd. is the labeler of record for MOSQUITO BUG OFF.

What form does MOSQUITO BUG OFF 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 MOSQUITO BUG OFF 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.

Has MOSQUITO BUG OFF 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.