Swimmers Support

Manufacturer
Newton Laboratories, Inc.
Effective date
2011-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:38:37

Label at a glance#

ProductSwimmers Support
Active ingredientAntimony Potassium Tartrate, Arnica Montana, Bellis Perennis, Bryonia Alba Root, Oyster Shell Calcium Carbonate, Crude, Capsicum, Chelidonium Majus, Copper, Digitalis, Drosera Rotundifolia Flowering Top, Lachesis Muta Venom, Lactic Acid, Dl-, Ledum Palustre Twig, Magnesium Carbonate, Manganese Acetate Tetrahydrate, Strychnos Nux-vomica Seed, Phytolacca Americana Root, Toxicodendron Pubescens Leaf, Ruta Graveolens Flowering Top, Lactic Acid, L-, Sulfuric Acid, Verbascum Thapsus, Vipera Berus Venom
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Swimmers Support   Formulated for symptoms associated with swimming and exposure to pool chemicals such as cramping, dry skin, fatigue and muscle soreness.

DOSAGE & ADMINISTRATION SECTION

Directions:  Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) as needed or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water.  Sensitive persons begin with 1 pellet and gradually increase to full dose .

OTC - ACTIVE INGREDIENT SECTION

Antimon. tart. 10x, Arnica 10x, Bellis 10x, Bryonia 10x, Calc. carb. 10x, Capsicum 10x, Chelidonium majus 10x, Cuprum met. 10x, Digitalis 10x, Drosera 10x, Lachesis 10x, Lacticum acidum 10x, Ledum 10x, Mag. carb. 10x, Mang. acet. 10x, Nux vom.10x, Phytolacca 10x, Rhus toxicodendron 10x, Ruta 10x, Sarcolacticum ac. 10x, Sulphuricum ac. 10x, Verbascum 10x, Vipera berus 10x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with swimming and exposure to pool chemicals such as cramping, dry skin, fatigue and muscle soreness.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.  

QUESTIONS SECTION

OTC - QUESTIONS SECTION

www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions?  1.800.448.7256

WARNINGS SECTION

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.  

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Antimony Potassium TartrateACTIVE INGREDIENTDL6OZ476V31
Arnica MontanaACTIVE INGREDIENTO80TY208ZW1
Bellis PerennisACTIVE INGREDIENT2HU33I03UY1
Bryonia Alba RootACTIVE INGREDIENTT7J046YI2B1
CapsicumACTIVE INGREDIENT00UK7646FG1
Chelidonium MajusACTIVE INGREDIENT7E889U5RNN1
CopperACTIVE INGREDIENT789U1901C51
DigitalisACTIVE INGREDIENTF1T8QT9U8B1
Drosera Rotundifolia Flowering TopACTIVE INGREDIENT75O014T1HG1
Lachesis Muta VenomACTIVE INGREDIENTVSW71SS07I1
Lactic Acid, Dl-ACTIVE INGREDIENT3B8D35Y7S41
Lactic Acid, L-ACTIVE INGREDIENTF9S9FFU82N1
Ledum Palustre TwigACTIVE INGREDIENT877L01IZ0P1
Magnesium CarbonateACTIVE INGREDIENT0E53J927NA1
Manganese Acetate TetrahydrateACTIVE INGREDIENT9TO51D176N1
Oyster Shell Calcium Carbonate, CrudeACTIVE INGREDIENT2E32821G6I1
Phytolacca Americana RootACTIVE INGREDIENT11E6VI8VEG1
Ruta Graveolens Flowering TopACTIVE INGREDIENTN94C2U587S1
Strychnos Nux-vomica SeedACTIVE INGREDIENT269XH139191
Sulfuric AcidACTIVE INGREDIENTO40UQP6WCF1
Toxicodendron Pubescens LeafACTIVE INGREDIENT6IO182RP7A1
Verbascum ThapsusACTIVE INGREDIENTC9TD27U1721
Vipera Berus VenomACTIVE INGREDIENT0ORO6NCA4M1
Antimony Cation (3+)ACTIVE MOIETY069647RPT51
Arnica MontanaACTIVE MOIETYO80TY208ZW1
Bellis PerennisACTIVE MOIETY2HU33I03UY1
Bryonia Alba RootACTIVE MOIETYT7J046YI2B1
CapsicumACTIVE MOIETY00UK7646FG1
Carbonate IonACTIVE MOIETY7UJQ5OPE7D1
Chelidonium MajusACTIVE MOIETY7E889U5RNN1
CopperACTIVE MOIETY789U1901C51
DigitalisACTIVE MOIETYF1T8QT9U8B1
Drosera Rotundifolia Flowering TopACTIVE MOIETY75O014T1HG1
Lachesis Muta VenomACTIVE MOIETYVSW71SS07I1
Lactic Acid, Dl-ACTIVE MOIETY3B8D35Y7S41
Lactic Acid, L-ACTIVE MOIETYF9S9FFU82N1
Ledum Palustre TwigACTIVE MOIETY877L01IZ0P1
ManganeseACTIVE MOIETY42Z2K6ZL8P1
Oyster Shell Calcium Carbonate, CrudeACTIVE MOIETY2E32821G6I1
Phytolacca Americana RootACTIVE MOIETY11E6VI8VEG1
Ruta Graveolens Flowering TopACTIVE MOIETYN94C2U587S1
Strychnos Nux-vomica SeedACTIVE MOIETY269XH139191
Sulfuric AcidACTIVE MOIETYO40UQP6WCF1
Toxicodendron Pubescens LeafACTIVE MOIETY6IO182RP7A1
Verbascum ThapsusACTIVE MOIETYC9TD27U1721
Vipera Berus VenomACTIVE MOIETY0ORO6NCA4M1
SucroseINACTIVE INGREDIENTC151H8M5541

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-111255714-1112-1, 55714-1112-2, 55714-1112-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SucroseSUCROSEC151H8M554CAPSULE, COATED PELLETS / ORAL59.8 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / SUBCUTANEOUS47.75 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / INTRAVENOUS1950 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS900 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554PASTILLE / ORAL426 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554WAFER / ORAL155.2 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS1 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554DROPS / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, EXTENDED RELEASE / ORAL284.54 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, EXTENDED RELEASE / ORAL619 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SOLUTION / ORAL38666 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CONCENTRATE / ORAL4800 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED, EXTENDED RELEASE / ORAL86 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, EMULSION / INTRAVENOUS970 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED, EXTENDED RELEASE / ORAL119.12 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SOLUTION / INTRAVENOUSNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, CHEWABLE / ORAL7258 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION / ORAL31885 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE / ORAL3568 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / RECTAL35.42 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554ELIXIR / ORAL18000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / TRANSMUCOSAL1255 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION / ORAL48209 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SOLUTION / ORAL42596 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / ORAL4249 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, COATED / ORAL516.42 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, DELAYED RELEASE / ORAL295.33 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / BUCCAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION, EXTENDED RELEASE / ORAL5400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS308 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTABLE, LIPOSOMAL / INTRAVENOUS7560 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS2000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL18790 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED / ORAL145 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, DELAYED RELEASE / ORAL955 mgExact identifier — unii candidate
48 equally ranked IID candidates

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
26fb001f-b633-acf5-e063-6294a90aeddeadfa208f-cc2a-b793-9569-124e251e8c8f2024-11-15WarningsExact identifier
spl set id: adfa208f-cc2a-b793-9569-124e251e8c8f

Reported adverse events (FAERS/openFDA)#

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