999 Itch Relief
FDA Label NDC 12753-930

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by China Resources Sanjiu Medical & Pharmaceutical Co Ltd for the product 999 Itch Relief (NDC 12753-930). 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, warnings, stop use and seek medical advice if, directions, other information, inactive ingredients, drug facts, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Menthol 1%

Camphor (synthetic) 1%

Dexamethasone Acetate 0.075%

Purpose

External Analgesic

External Analgesic

Anti-allergic

Warnings

For external use only. Avoid contact with the eyes. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children.

Stop Use And Seek Medical Advice If

Condition worses. Symptoms persisit for more than 7 days. Symptoms clear up and occur again within a few days. Excessive irritation of the skin develops.

Directions

Pregnant and children under 2 years of age. Do not use, consult a doctor.

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.

Other Information

Keep in a lightly closed container. Store at 8 to 30 degree centigrade (46-86 Fahrenheit) in a dry plac away from sunlight.

Inactive Ingredients

Hexadecanolactone

Ethylparaben

Glycerin

Glycertyl Monostearate

Drug Facts

Carton (Carton)

Carton (Carton)

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