SHING-RELEEV- benzalkonium chloride liquid

Drug Labeling and Warnings

Drug Details [pdf]

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.

DOSAGE & ADMINISTRATION

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)

PRINCIPAL DISPLAY PANEL

Shing carton

INGREDIENTS AND APPEARANCE

SHING-RELEEV  
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63287-420
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1 mL
Allantoin (UNII: 344S277G0Z) (Allantoin - UNII:344S277G0Z)	Allantoin	5 mg  in 1 mL
Benzyl Alcohol (UNII: LKG8494WBH) (Benzyl Alcohol - UNII:LKG8494WBH)	Benzyl Alcohol	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Methylparaben (UNII: A2I8C7HI9T)
Potassium Sorbate (UNII: 1VPU26JZZ4)
Propylparaben (UNII: Z8IX2SC1OH)
Echinacea purpurea flowering top (UNII: 2EMS3QFX65)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63287-420-02	1 in 1 BOX
1	NDC: 63287-420-01	60 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/14/2010

Labeler - Merix Pharmaceutical Corp. (158385687)

Registrant - Topical Pharmaceutiocals Inc. (831530683)

Establishment
Name	Address	ID/FEI	Business Operations
Topical Pharmaceutiocals Inc.		831530683	manufacture(63287-420)