ULTRA PRO

Manufacturer
SENA LLC | Newton Laboratories, Inc.
Effective date
2012-07-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:04:23

Label at a glance#

ProductULTRA PRO
Active ingredientArtemisia Abrotanum Flowering Top, Semecarpus Anacardium Juice, Barium Chloride Dihydrate, Oyster Shell Calcium Carbonate, Crude, Tribasic Calcium Phosphate, Fucus Vesiculosus, Graphite, Helleborus Niger Root, Bos Taurus Hypothalamus, Strychnos Ignatii Seed, Lycopodium Clavatum Spore, Magnesium Phosphate, Dibasic Trihydrate, Claviceps Purpurea Sclerotium, Silicon Dioxide, Solidago Virgaurea Flowering Top, Thymus Serpyllum, Thyroid, Unspecified
Label structure11 sections

Dosage and administration

Swirl or shake bottle 5 times prior to use. Apply three sprays under the tongue twice daily, upon awakening and before sleeping. Do not eat, drink, or brush your teeth within 5 minutes before or after taking this product. Consult a physician prior to use in children under 15 years of age.

Storage and handling

Store in a cool dry place. Tamper-evident for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Abrotanum 10X, Anacard or. 10X, Baryta mur. 10X, Calc. carb. 10X, Calc. phos. 10X, Fucus vesiculosus 10X, Graphites 10X, Hellebor nig. 10X, Hypothalamus 15X, Ignatia 10X, Lycopodium 10X, Magnesia phos. 10X, Secale 10X, Silicea 10X, Solidago virgaurea 10X, Thyroidinum 15X, Thymus serpyllum 10X

Indications

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with: hunger cravings, overeating, obesity, overweight, adipose storage, excessive appetite, cravings for sweets & starches, abdominal fat.

Warnings

WARNINGS SECTION

Stop use and ask a doctor if symptoms persist or worsen.

Overdose

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Take only on advice of physician.

 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Swirl or shake bottle 5 times prior to use. Apply three sprays under the tongue twice daily, upon awakening and before sleeping. Do not eat, drink, or brush your teeth within 5 minutes before or after taking this product. Consult a physician prior to use in children under 15 years of age.

Inactive ingredients

INACTIVE INGREDIENT SECTION

USP Purified water, USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%

Other Information

STORAGE AND HANDLING SECTION

Store in a cool dry place.

Tamper-evident for your protection. Use only if safety seal is intact.

Questions

OTC - QUESTIONS SECTION

866-891-2002

SozaClinic.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 55924-2001-1

SOZA CLINIC

ULTRA PRO

Weight Loss and Cravings Control

Homeopathics For Professional Use Only

1 FL OZ (29.6 ml)

Manufactured in the USA for:
SOZA CLINIC
677 West DeKalb Pike, 2nd Floor
King of Prussia, PA 19406
866-891-2002 | SozaClinic.com

ULTRA PRO Label
ULTRA PRO Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55924-2001-12020-01-31C16284748780-19d75b9d1-0b46-f424-e053-dadaa90a57ceUltra Pro

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55924-2001-1ULTRA PRO1 mL in 1 BOTTLELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55924-2001ULTRA PRO (ARTEMISIA ABROTANUM FLOWERING TOP, SEMECARPUS ANACARDIUM JUICE, BARIUM CHLORIDE DIHYDRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, FUCUS VESICULOSUS, GRAPHITE, HELLEBORUS NIGER ROOT, BOS TAURUS HYPOTHALAMUS, STRYCHNOS IGNATII SEED, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, CLAVICEPS PURPUREA SCLEROTIUM, SILICON DIOXIDE, SOLIDAGO VIRGAUREA FLOWERING TOP, THYMUS SERPYLLUM AND THYROID, UNSPECIFIED) LIQUID [SENA LLC]1Legacy NDC, 1 package rows20130320_9180f51a-ba45-191a-3127-b3b85330a6b6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Artemisia Abrotanum Flowering TopACTIVE INGREDIENTQG07G580U01
Barium Chloride DihydrateACTIVE INGREDIENTEL5GJ3U77E1
Bos Taurus HypothalamusACTIVE INGREDIENTS6G2NLH4Y71
Claviceps Purpurea SclerotiumACTIVE INGREDIENT01G9XEA93N1
Fucus VesiculosusACTIVE INGREDIENT535G2ABX9M1
GraphiteACTIVE INGREDIENT4QQN74LH4O1
Helleborus Niger RootACTIVE INGREDIENT608DGJ68151
Lycopodium Clavatum SporeACTIVE INGREDIENTC88X29Y4791
Magnesium Phosphate, Dibasic TrihydrateACTIVE INGREDIENTHF539G9L3Q1
Oyster Shell Calcium Carbonate, CrudeACTIVE INGREDIENT2E32821G6I1
Semecarpus Anacardium JuiceACTIVE INGREDIENTY0F0BU8RDU1
Silicon DioxideACTIVE INGREDIENTETJ7Z6XBU41
Solidago Virgaurea Flowering TopACTIVE INGREDIENT5405K23S501
Strychnos Ignatii SeedACTIVE INGREDIENT1NM3M2487K1
Thymus SerpyllumACTIVE INGREDIENT86H4S6K51N1
Thyroid, UnspecifiedACTIVE INGREDIENT0B4FDL9I6P1
Tribasic Calcium PhosphateACTIVE INGREDIENT91D9GV0Z281
Artemisia Abrotanum Flowering TopACTIVE MOIETYQG07G580U01
Barium CationACTIVE MOIETYV645272HLN1
Bos Taurus HypothalamusACTIVE MOIETYS6G2NLH4Y71
Calcium CationACTIVE MOIETY2M83C4R6ZB1
Claviceps Purpurea SclerotiumACTIVE MOIETY01G9XEA93N1
Fucus VesiculosusACTIVE MOIETY535G2ABX9M1
GraphiteACTIVE MOIETY4QQN74LH4O1
Helleborus Niger RootACTIVE MOIETY608DGJ68151
Lycopodium Clavatum SporeACTIVE MOIETYC88X29Y4791
Magnesium CationACTIVE MOIETYT6V3LHY8381
Oyster Shell Calcium Carbonate, CrudeACTIVE MOIETY2E32821G6I1
Semecarpus Anacardium JuiceACTIVE MOIETYY0F0BU8RDU1
Silicon DioxideACTIVE MOIETYETJ7Z6XBU41
Solidago Virgaurea Flowering TopACTIVE MOIETY5405K23S501
Strychnos Ignatii SeedACTIVE MOIETY1NM3M2487K1
Thymus SerpyllumACTIVE MOIETY86H4S6K51N1
Thyroid, UnspecifiedACTIVE MOIETY0B4FDL9I6P1
AlcoholINACTIVE INGREDIENT3K9958V90M1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55924-200155924-2001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
AlcoholALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAVENOUS6405 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION / INTRAMUSCULAR1491 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL, METERED / TRANSDERMAL3675 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MDROPS / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION, CONCENTRATE / INTRAVENOUS4000 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION, SOLUTION / SUBCUTANEOUS6.1 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY, METERED / SUBLINGUAL29 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MJELLY / VAGINALNAExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / INTRAVESICAL7892 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / INTRAVENOUS99 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSUSPENSION / RECTAL0.35 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL / RECTAL898 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAMUSCULAR1000 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / TRANSDERMAL49.37 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MMOUTHWASH / BUCCAL200 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, METERED / NASAL70 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION / SUBCUTANEOUS149 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION / INTRAVASCULAR100 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / INTRAVENOUS400 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MCONCENTRATE / BUCCAL679 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / INTRAMUSCULAR400 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION / INTRAVENOUS92 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MPASTE / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MGEL / TRANSDERMAL7360 mgExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MSOLUTION / DENTAL12.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
AlcoholALCOHOL3K9958V90MINJECTION, EMULSION / INTRAVENOUS520 mgExact identifier — unii candidate
59 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
4f696521-921a-4fb8-0d0d-7ddd368a6e4a9180f51a-ba45-191a-3127-b3b85330a6b62012-07-24WarningsExact identifier
spl id: 4f696521-921a-4fb8-0d0d-7ddd368a6e4a
spl set id: 9180f51a-ba45-191a-3127-b3b85330a6b6

Reported adverse events (FAERS/openFDA)#

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