Amolg A
FDA Label NDC 72689-0033

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oasis Trading for the product Amolg A (NDC 72689-0033). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Purpose

temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, poison ivy, poison oak, or poison sumac soaps detergents, cosmetics, jewelry, seborrheic dermatitis, psoriasis, external genital and anal itching

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

Warnings

Do not use in the eyes by putting this product into the rectum by using fingers or any mechanical device or applicator
Ask a doctor before use if you have a vaginal discharge rectal bleeding
diaper rash
When using this product consult a doctor before exceeding recommended dosage
Stop use and ask a doctor if condition gets worse condition persists for more than 7 days
condition clears up and occurs again within a few days. Do not begin to use any other hydrocortisone product unless you have consulted a doctor.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

cetostearyl alcohol, propylene glycol, purified water, sodium lauryl sulfate, white petrolatum

Dosage & Administration

For external use only

Package Label.Principal Display Panel

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