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999 ITCH RELIEF

Medically reviewed by Drugs.com. Last updated on Oct 12, 2021.

Dosage form: ointment
Ingredients: MENTHOL 200mg in 20000mg, CAMPHOR (SYNTHETIC) 200mg in 20000mg, DEXAMETHASONE 15mg in 20000mg
Labeler: China Resources Sanjiu Medical & Pharmaceutical Co Ltd
NDC Code: 12753-930

999 ITCH RELIEF OINTMENT

ACTIVE INGREDIENTS

Menthol 1%

Camphor (synthetic) 1%

Dexamethasone Acetate 0.075%

Purpose

External Analgesic

External Analgesic

Anti-allergic

For the temporary relief of pain caused by itching and rashes, poison ivy, poison oak

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 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.

Warnings

Keep out of reach of children.

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.

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

999 ITCH RELIEF 
menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12753-930
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL200 mg  in 20000 mg
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC)200 mg  in 20000 mg
DEXAMETHASONE (DEXAMETHASONE) DEXAMETHASONE15 mg  in 20000 mg
Inactive Ingredients
Ingredient NameStrength
HEXADECANOLACTONE 
Ethylparaben 
Glycerin 
Glyceryl Monostearate 
Packaging
#Item CodePackage Description
1NDC:12753-930-1920000 mg in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/03/2003
Labeler - China Resources Sanjiu Medical & Pharmaceutical Co Ltd (544695711)
Registrant - China Resources Sanjiu Medical & Pharmaceutical Co Ltd (544695711)
Establishment
NameAddressID/FEIOperations
China Resources Sanjiu Medical & Pharmaceutical Co Ltd544695711manufacture(12753-930)

 
China Resources Sanjiu Medical & Pharmaceutical Co Ltd

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.