Deeveeant Numb

Deeveeant Numb is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Valekista Limited taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71383-014, application part348, label effective 20170706. It is one of 152 FDA drug label records sharing the active ingredient LIDOCAINE. 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 LIDOCAINE are most often described in connection with: temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use For the temporary relief of pain

Directions Adults and children 2 years and older clean the affected area apply to affected area not more than 3 to 4 times daily remove residue if desired Children under 2 years old: Consult a doctor

Warnings For external use only Avoid contact with eyes Not for prolonged use Do not use in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clears up and occurs again within a few days rash or irritation develops, persists or increases 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: 800-222-1222

FDA lists 152 drug label records with LIDOCAINE 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 Deeveeant Numb used for?
Use For the temporary relief of pain

Who makes Deeveeant Numb?
Valekista Limited is the labeler of record for Deeveeant Numb. 152 FDA label records share the active ingredient LIDOCAINE, 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 Deeveeant Numb 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 Deeveeant Numb 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 LIDOCAINE?
Yes. 152 FDA drug label records list LIDOCAINE 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 Deeveeant Numb 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.