Ivy-Dry Super

Ivy-Dry Super is an FDA-registered drug product whose active ingredient is BENZYL ALCOHOL, CAMPHOR, MENTHOL. It is labelled by Ivy-Dry, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 49546-106, application part348, label effective 20171227. 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 BENZYL ALCOHOL, CAMPHOR, MENTHOL are most often described in connection with: temporary relief, itching associated, insect bites, minor skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses for the temporary relief of itching associated with insect bites and minor skin irritations

Directions Apply to affected area not more than 3 times daily. Children under 6 years of age: do not use, ask a doctor. Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary. Test product on small patch of skin before applying to the entire body.

For external use only. Do not use on face or genital areas on areas of blistered or broken skin with a compress after application When using this product do not get into eyes if contact occurs, flush eyes with water Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding, ask a doctor before use. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

What is Ivy-Dry Super used for?
Uses for the temporary relief of itching associated with insect bites and minor skin irritations

Who makes Ivy-Dry Super?
Ivy-Dry, Inc. is the labeler of record for Ivy-Dry Super.

What form does Ivy-Dry Super 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 Ivy-Dry Super 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 Ivy-Dry Super 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.