Instant Cooling Itch Relief

Instant Cooling Itch Relief is an FDA-registered drug product whose active ingredient is HYDROCORTISONE. It is labelled by CVS Pharmacy taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 51316-388, application M017, label effective 20260807. It is one of 81 FDA drug label records sharing the active ingredient HYDROCORTISONE. 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 HYDROCORTISONE are most often described in connection with: temporarily relieves, itching associated, minor skin, irritation inflammation, rashes due, eczema psoriasis, insect bites, poison ivy. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves itching associated with minor skin irritation, inflammation and rashes due to: eczema psoriasis insect bites poison ivy, oak, and sumac soaps and detergents seborrheic dermatitis cosmetics jewelry other use of this product hsould only be under the advice and supervision of a doctor

Directions shake well adults and children 2 years of age and older: apply to affected area, not more than 3 to 4 times daily to apply to face, spray into palm of hand and gently apply children under 2 years of age: Do not use, ask a doctor

Warnings For external use only. Flammable: Do not use while smoking or near heat or flame Do not use in or near eyes for the treatment of diaper rash, consult a doctor When using this product keep out of eyes. Rinse with warm water to remove. contents under pressure do not puncture or incinerate. use only as directed do not use more than directed unless told to do so by a doctor Stop use and ask a doctor if condition worsens or does not improve within 7 days symptoms persist for more than 7 days or clear up and occur again within a few days, stop use of this product and do not begin use of any other hydrocortisone product unless you have consulted a doctor If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 81 drug label records with HYDROCORTISONE 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 Instant Cooling Itch Relief used for?
Uses temporarily relieves itching associated with minor skin irritation, inflammation and rashes due to: eczema psoriasis insect bites poison ivy, oak, and sumac soaps and detergents seborrheic dermatitis cosmetics jewelry other use of this product hsould only be under the advice and supervision of a doctor

Who makes Instant Cooling Itch Relief?
CVS Pharmacy is the labeler of record for Instant Cooling Itch Relief. 81 FDA label records share the active ingredient HYDROCORTISONE, 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 Instant Cooling Itch Relief 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 Instant Cooling Itch Relief 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 HYDROCORTISONE?
Yes. 81 FDA drug label records list HYDROCORTISONE 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 Instant Cooling Itch Relief 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.