Shingles Control

Manufacturer
Forces of Nature
Effective date
2011-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:07

Label at a glance#

ProductShingles Control Extra Strength
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, HYPERICUM PERFORATUM, SODIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply to affected area at first sign of an outbreak 3-5 times per day. Avoid contact with eyes.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active Ingredients*
Equal parts of:
Purpose
Calendula Officinalis 8X HPUSPromotes healthy skin
Natrum Muriaticum 8X HPUS Remedy for herpes, skin eruptions, hives
Hypericum Perforatum 8X HPUSFor herpes zoster/shingles

* The letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homœopathic Pharmacopœia of the United States.

Also Includes

INACTIVE INGREDIENT SECTION

Certified Organic Oils of: Eucalypus Radiata Leaf, French Lavandin Super, Napalese Palmarosa, Tea Tree, Pelargonium Graveolens Leaf, Cypress

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area at first sign of an outbreak 3-5 times per day. Avoid contact with eyes.

Indications

INDICATIONS & USAGE SECTION

For relief and treatment of skin inflammation, pain and redness of shingles outbreaks.

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

Product Note: Shingles is a viral infection (herpes zoster) of the skin with symptoms of rashes or blisters, redness and pain. Viral infections are often highly contagious.

OTC - ASK DOCTOR SECTION

If skin symptoms worsen consult a health care professional.

OTC - STOP USE SECTION

Some individuals may be sensitive to tea tree or other oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - DO NOT USE SECTION

External use only. If accidental ingestion, get medical help or contact a Poison Control Center.

Do not apply to the eyes or mucous membranes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep all medicines out of the reach of children.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or symptoms last more than 7 days or clear up and occur again within a few days.

PRINCIPAL DISPLAY PANEL - 11ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FORCES OF NATURE ®

Shingles
CONTROL
EXTRA STRENGTH

HOMEOPATHIC
MEDICINE
FDA REGISTERED
+
USDA
ORGANIC

11ml

PRINCIPAL DISPLAY PANEL - 11ml Bottle Label
PRINCIPAL DISPLAY PANEL - 11ml Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51393-7323-12019-10-29C16284748780-1960f7f55-d178-8e05-e053-dbdaa90a074aShingles Control Extra Strength
51393-7323-22019-10-29C16284748780-1960f7f55-d178-8e05-e053-dbdaa90a074aShingles Control Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-7323-1Shingles Control Extra Strength11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS111
51393-7323-2Shingles Control Extra Strength33 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS331

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51393-7323SHINGLES CONTROL (CALENDULA OFFICINALIS FLOWERING TOP, HYPERICUM PERFORATUM, AND SODIUM CHLORIDE) SOLUTION/ DROPS [FORCES OF NATURE]1Legacy NDC, 2 package rows20110406_2018e47d-9851-415f-8cb8-37326489b73e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALENDULA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT18E7415PXQ1
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
CALENDULA OFFICINALIS FLOWERING TOPACTIVE MOIETY18E7415PXQ1
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI6621
GERANIUM OIL, ALGERIAN TYPEINACTIVE INGREDIENT5Q1I94P4WG1
LAVANDIN OILINACTIVE INGREDIENT9RES347CKG1
PALMAROSA OILINACTIVE INGREDIENT0J3G3O53ST1
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51393-732351393-7323-1, 51393-7323-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
675f6a97-2d8b-443b-ae99-fa314e16aaa42018e47d-9851-415f-8cb8-37326489b73e2011-03-31WarningsExact identifier
spl id: 675f6a97-2d8b-443b-ae99-fa314e16aaa4
spl set id: 2018e47d-9851-415f-8cb8-37326489b73e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.