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shing-Releev by Topical Pharmaceuticals Inc.

Dosage form: liquid
Ingredients: Benzalkonium Chloride 1.3mL in 1mL, Allantoin 5mL in 1mL, Benzyl Alcohol 5mL in 1mL
Labeler: Topical Pharmaceuticals Inc.
NDC Code: 15478-005

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.


ACTIVE INGREDIENTS: Benzalkanium Chloride .13%
Allantoin .5%
Benzyl Alcohol .5%


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.


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 .


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 approved.jpg

benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15478-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride1.3 mL  in 1 mL
Allantoin (Allantoin) Allantoin5 mL  in 1 mL
Benzyl Alcohol (Benzyl Alcohol) Benzyl Alcohol5 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Potassium Sorbate 
Echinacea purpurea flowering top 
#Item CodePackage Description
1NDC:15478-005-021 BOTTLE, SPRAY (BOTTLE) in 1 BOX
1NDC:15478-005-0160 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/14/2010
Labeler - Topical Pharmaceuticals Inc. (831530683)

Topical Pharmaceuticals Inc.

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Medically reviewed on Nov 2, 2018

Further information

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