Country: United States
Language: English
Source: NLM (National Library of Medicine)
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y), Allantoin (UNII: 344S277G0Z) (Allantoin - UNII:344S277G0Z), Benzyl Alcohol (UNII: LKG8494WBH) (Benzyl Alcohol - UNII:LKG8494WBH)
Merix Pharmaceutical Corp.
OTC DRUG
For the relive of symtoms associated with shingles including pain, Burning, Itching and tingling First aid to help guard against secondary skin infection due to shingles.
OTC monograph not final
SHING-RELEEV - BENZALKONIUM CHLORIDE LIQUID MERIX PHARMACEUTICAL CORP. _Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they_ _comply with applicable regulations and policies. FDA has not evaluated whether this product complies._ ---------- DRUGS FACTS ACTIVE INGREDIENTS: Benzalkanium Chloride .13% Allantoin .5% Benzyl Alcohol .5% USES: For the relive of symtoms associated with shingles including pain, Burning, Itching and tingling First aid to help guard against secondary skin infection due to shingles. WARNINGS: For external used only. Not for ingestion. DO NOT USED- in yeast infections- do not spray directly on the eyes WHEN USING THIS PRODUCT, may tingle on contact. STOP USED AND ASK DOCTOR IF - condition worsens- symptoms last more then 7 days . KEEP OUT OF REACH OF CHILDREN: If swallowget medical help or contact a Poison Control Center right away. DIRECTIONS: Use at first sign of irritation or itching. Adults and children 12 years or older. Clean without soap. apply liberally to clean dry area free of soap or cleanser residue. Apply to area as needed 3-4 times daily. Do not use cotton applicator. May be used with sterile bandage after area is dry. OTHER INGREDIENTS .Methylparaben Potassium Sorbate (natural preservative ). Propylparaben , Viracea (proprietary Echinacea purpurea extract), water (purified) Shing carton SHING-RELEEV Merix Pharmaceutical Corp. benzalkonium chloride liquid PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:6 328 7-420 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH BENZA LKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (Benzalko nium - UNII:7N6 JUD5X6 Y) Benzalko nium Chlo ride 1.3 mg in 1 mL ALLA NTO IN (UNII: 344S277G0 Z) (Allanto in - UNII:344S277G0 Z) Alla nto in 5 mg in 1 mL BENZYL ALCO HO L (UNII: LKG8 49 4WBH) (Benzyl Alco ho l - UNII:LKG8 49 4WBH) Benzyl Alco ho l 5 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WA TER (UNII: 0 59 QF0 KO0 R Read the complete document