TERRASIL SHINGLES TREATMENT MAXIMUM STRENGTH- ranunculus bulbosus and sodium chloride ointment 
Aidance Skincare & Topical Solutions, LLC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Drug Facts

Active Ingredients

Natrum Muriaticum, Ranunculus Bulbosus

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States

Purpose

Natrum Muriaticum - Zoster Shingle Symptom Relief

Ranunculus Bulbosus - Zoster Shingle Blisters, Stinging Pain

Uses

Symptomatic treatment of shingles

Warnings

For external use only.
Virally based infections are contagious. This product will not stop the spread of viral infections.
Do not use - in the eyes - over large areas of the body - if you are allergic to any ingredient in this product.
Ask a doctor before use if pregnant or nursing.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

Keep out of reach of children.

If swallowed, call poison control or seek medical help.

Directions

Wash and dry affected skin. Apply a thin layer of Terrasil. Repeat procedure 2-3 times daily until outbreak is relieved. Store at room temperature.

Inactive Ingredients

cera alba (organic beeswax), juniperus virginiana (cedarwood) oil, magnesium oxide, palmarosa oil, silver oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide

PRINCIPAL DISPLAY PANEL - 44g Label

terrasil

Shingles Treatment
Fast - Soothing - All-Natural

Jar Label

TERRASIL SHINGLES TREATMENT  MAXIMUM STRENGTH
natrum muriaticum, ranunculus bulbosus ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24909-141
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS10 [hp_X]  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE3 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
JOJOBA OIL (UNII: 724GKU717M)  
JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)  
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)  
PALMAROSA OIL (UNII: 0J3G3O53ST)  
SILVER OXIDE (UNII: 897WUN6G6T)  
WHITE WAX (UNII: 7G1J5DA97F)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24909-141-1414 g in 1 JAR; Type 0: Not a Combination Product
2NDC:24909-141-4444 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic10/11/201204/24/2015
Labeler - Aidance Skincare & Topical Solutions, LLC (018950611)
Establishment
NameAddressID/FEIBusiness Operations
Aidance Skincare & Topical Solutions, LLC018950611manufacture(24909-141) , label(24909-141)

Revised: 7/2015
 
Aidance Skincare & Topical Solutions, LLC