DO ME DELAY

DO ME DELAY is an FDA-registered drug product whose active ingredient is LIDOCAINE HCL. It is labelled by Prodigy Media Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 70171-0051, application M017, label effective 20260521. It is one of 11 FDA drug label records sharing the active ingredient LIDOCAINE HCL. 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 HCL are most often described in connection with: temporary relief, itching associated, sunburns minor, cuts insect, skin irritations. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

For the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations

Directions Adulls 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 physician.

Warnings . For external use only. . Avoid contact with eyes Stop use and ask a doctor if . Condition worsens or symptoms persist for more than 7 days . Symploms clear up and occur again within a few days . Do not use in large quantities, particulary over raw surfaces or blistered areas. Do not exceed the recommended daily dosage unless directed by a doctor. Do not use . On wounds or damaged skin.

FDA lists 11 drug label records with LIDOCAINE HCL 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 DO ME DELAY used for?
For the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations

Who makes DO ME DELAY?
Prodigy Media Inc is the labeler of record for DO ME DELAY. 11 FDA label records share the active ingredient LIDOCAINE HCL, 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 DO ME DELAY 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 DO ME DELAY 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 HCL?
Yes. 11 FDA drug label records list LIDOCAINE HCL 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 DO ME DELAY 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.