Drugplain

QC Medicated anti itch 1 g/100g

Pramoxine hydrochloride, menthol · CREAM · Chain Drug Marketing Association

No Recall History
Plain English

QC Medicated anti itch is a cream containing pramoxine hydrochloride, menthol at 1 g/100g, taken topical. Manufactured by Chain Drug Marketing Association.

Key Facts

Brand Name
QC Medicated anti itch
Generic Name
Pramoxine hydrochloride, menthol
NDC Code (Product)
63868-959
Manufacturer
Chain Drug Marketing Association
Strength
1 g/100g
Dosage Form
CREAM
Route
TOPICAL
Marketing Status
Application #
M017
Marketing Start
12/07/2020

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses for the temporary relief of pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations ,minor rashes due to poison ivy, poison oak, or poison sumac

Dosage & Administration

Dosage Adults and Children 2 years and older: Apply to affected are not more than 3 to 4 times daily.

Warnings

Warnings For external use only When using this product do not get into eyes Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is QC Medicated anti itch used for?

QC Medicated anti itch contains Pramoxine hydrochloride, menthol. It is a cream taken topical. Consult your doctor for specific uses.

Is QC Medicated anti itch a controlled substance?

QC Medicated anti itch is not classified as a controlled substance by the DEA.

What is the generic name for QC Medicated anti itch?

The generic name for QC Medicated anti itch is Pramoxine hydrochloride, menthol. There are 6 other brand versions of Pramoxine hydrochloride, menthol.

What is the NDC code for QC Medicated anti itch 1 g/100g?

The NDC (National Drug Code) for QC Medicated anti itch 1 g/100g is 63868-959, listed by Chain Drug Marketing Association.