FDA.reportPublic FDA data

No Sweat Anti Perspirant

Manufacturer
King Bio Inc.
Effective date
2012-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:04:01

Label at a glance#

ProductNo Sweat Anti Perspirant
Active ingredientANTIMONY POTASSIUM TARTRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CINCHONA OFFICINALIS BARK, MERCURIUS SOLUBILIS, PILOCARPUS JABORANDI LEAF, PHOSPHORIC ACID, SAMBUCUS NIGRA FLOWERING TOP, SILICON DIOXIDE, SULFURIC ACID
Label structure8 sections

Indications and uses

Uses for temporary internal control of excessive perspiration.

Dosage and administration

Directions Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed. Adult Dose 3 pump sprays Children 2 - 12 years 2 pump sprays

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Official HPUS: Antimonium tartaricum, Calcarea carbonica, Cinchona officinalis, Mercurius solubilis, Mercurius vivus, Pilocarpus, Phosphoricum acidum, Sambucus nigra, Silicea and Sulphuricum acidum.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base: 10X, 30X, and LM1 potencies.

Purpose

OTC - PURPOSE SECTION


Uses for temporary internal control of excessive perspiration.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION


Directions Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed.

Adult Dose 3 pump sprays

Children 2 - 12 years 2 pump sprays

Warnings

WARNINGS SECTION

If symptoms persist or worsen, consult a physician. If pregnant or nursing, take only on advice of healthcare professional. Keep out of reach of children.

Other: Tamper resistant for your protection. Use only if safety seal is intact.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of children.

Indications and Usage

INDICATIONS & USAGE SECTION

Uses for temporary internal control of excessive perspiration.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of label
Image of label

King Bio Inc.

3 Westside Drive

Asheville, NC 28806

Questions? Call 800.543.3245

www.kingbio.com

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5085-22020-01-31C16284748780-19d75b9d0-eb42-f424-e053-dadaa90a57ceNo Sweat Anti-Perspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5085-2No Sweat Anti Perspirant59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5085NO SWEAT ANTI PERSPIRANT (ANTIMONIUM TARTARICUM, CALCAREA CARBONICA, CINCHONA OFFICINALIS, MERCURIUS SOLUBILIS, MERCURIUS VIVUS, PILOCARPUS, PHOSPHORICUM ACIDUM, SAMBUCUS NIGRA, SILICEA AND SULPHURICUM ACIDUM) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20121012_272ab49b-0be5-4ab7-b6c7-253045817e08.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONY POTASSIUM TARTRATEACTIVE INGREDIENTDL6OZ476V31
CINCHONA OFFICINALIS BARKACTIVE INGREDIENTS003A158SB1
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G21
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
PILOCARPUS JABORANDI LEAFACTIVE INGREDIENT26ZE1BZ2US1
SAMBUCUS NIGRA FLOWERING TOPACTIVE INGREDIENTCT03BSA18U1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SULFURIC ACIDACTIVE INGREDIENTO40UQP6WCF1
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT51
CINCHONA OFFICINALIS BARKACTIVE MOIETYS003A158SB1
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G21
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I1
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
PILOCARPUS JABORANDI LEAFACTIVE MOIETY26ZE1BZ2US1
SAMBUCUS NIGRA FLOWERING TOPACTIVE MOIETYCT03BSA18U1
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
SULFURIC ACIDACTIVE MOIETYO40UQP6WCF1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-508557955-5085-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANTIMONY POTASSIUM TARTRATEDL6OZ476V3ACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
CINCHONA OFFICINALIS BARKS003A158SBACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
PILOCARPUS JABORANDI LEAF26ZE1BZ2USACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
SAMBUCUS NIGRA FLOWERING TOPCT03BSA18UACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SULFURIC ACIDO40UQP6WCFACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
cd04a41c-792e-45d1-885d-5e9e65ad2037272ab49b-0be5-4ab7-b6c7-253045817e082012-09-17WarningsExact identifier
spl id: cd04a41c-792e-45d1-885d-5e9e65ad2037
spl set id: 272ab49b-0be5-4ab7-b6c7-253045817e08

Reported adverse events (FAERS/openFDA)#

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