Active Ingredients
Hydrocortisone 1.0%
999 Itch Relieving
FDA Label NDC 69436-931
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Cr. Shunfeng Pharmaceutical Co Ltd for the product 999 Itch Relieving (NDC 69436-931). 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 active ingredients, purpose, use, warnings, stop use and seek medical advice if, directions, keep out of reach of children., other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-Itch
Use
For the temporary relief of itching associated with minor skin irritations, inflammation and rashes due to: cosmetics, insect bites, psoriasis, eczema, seborrheic dermatitis.
Warnings
For external use only. Avoid contact with the eyes. If swallowed, get medical help or contact a Poison Control Center right away.
Stop Use And Seek Medical Advice If
Condition worsens. Symptoms persist for more than 7 days. Symptoms clear up and occur again within a few days. Excessive irritation of the skin develops.
Directions
Adult and children 2 years of age and older. Apply liberally to affected area not more than 5 times daily and 5-8 times per day for some severe cases or follow doctor's instruction.
Keep Out Of Reach Of Children.
Other Information
Keep in a tightly closed container. Store at 8 to 30 ℃ (46-86℉) in a dry place away from sunlight.
You may report serious side effects to: 1452 W. Holt Ave, Pomona, CA 91768
Inactive Ingredients
Glyceryl Monostearate, Glyceryl Distearate, Glycerin, Stearic Acid, White Petrolatum, Ethylparaben, Sodium Lauryl Sulfate, Water
Drug Facts
Image Description (Carton)
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