Ultra Advantage

Product NDC
69727-0003
11-digit product format
697270003
Labeler code
69727
Product ID
69727-0003_9381b435-2410-4ca1-8895-078e4475e808
Type
HUMAN OTC DRUG
Nonproprietary name
Abrotanum (Artemisia Abrotanum), Anacardium Orientale, Fucus Vesiculosus, Helleborus Niger, Hypothalamus Suis, Lycopodium Clavatum, Thymolum, Thymus Serpyllum, Thyroidinum (Bovine), Glandula Suprarenalis Suis, Hepar Suis, Pancreas Suis, Cinchona Officinalis, Nicotinamidum, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Magnesia Phosphorica, Solidago Virgaurea, Graphites
Dosage form
LIQUID
Route
ORAL
Labeler
ELTTAC Inc DBA SWL
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-09-03
Substance
ARTEMISIA ABROTANUM FLOWERING TOP; SEMECARPUS ANACARDIUM JUICE; FUCUS VESICULOSUS; HELLEBORUS NIGER ROOT; SUS SCROFA HYPOTHALAMUS; LYCOPODIUM CLAVATUM SPORE; THYMOL; THYMUS SERPYLLUM WHOLE; THYROID, BOVINE; SUS SCROFA ADRENAL GLAND; PORK LIVER; SUS SCROFA PANCREAS; CINCHONA OFFICINALIS BARK; NIACINAMIDE; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SOLIDAGO VIRGAUREA FLOWERING TOP; GRAPHITE
Active strength
8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Ultra Advantage
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARTEMISIA ABROTANUM FLOWERING TOP8 [hp_X]/mL
SEMECARPUS ANACARDIUM JUICE8 [hp_X]/mL
FUCUS VESICULOSUS8 [hp_X]/mL
HELLEBORUS NIGER ROOT8 [hp_X]/mL
SUS SCROFA HYPOTHALAMUS8 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE8 [hp_X]/mL
THYMOL8 [hp_X]/mL
THYMUS SERPYLLUM WHOLE8 [hp_X]/mL
THYROID, BOVINE8 [hp_X]/mL
SUS SCROFA ADRENAL GLAND8 [hp_X]/mL
PORK LIVER8 [hp_X]/mL
SUS SCROFA PANCREAS8 [hp_X]/mL
CINCHONA OFFICINALIS BARK8 [hp_X]/mL
NIACINAMIDE8 [hp_X]/mL
BARIUM CARBONATE12 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]/mL
TRIBASIC CALCIUM PHOSPHATE12 [hp_X]/mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE12 [hp_X]/mL
SOLIDAGO VIRGAUREA FLOWERING TOP12 [hp_X]/mL
GRAPHITE12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 20 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
QG07G580U0Internal UNII lookup
Y0F0BU8RDUInternal UNII lookup
535G2ABX9MInternal UNII lookup
608DGJ6815Internal UNII lookup
N6R0856Z79Internal UNII lookup
C88X29Y479Internal UNII lookup
3J50XA376EInternal UNII lookup
86H4S6K51NInternal UNII lookup
MN18OTN73WInternal UNII lookup
398IYQ16YVInternal UNII lookup
6EC706HI7FInternal UNII lookup
9Y3J3362RYInternal UNII lookup
S003A158SBInternal UNII lookup
25X51I8RD4Internal UNII lookup
6P669D8HQ8Internal UNII lookup
2E32821G6IInternal UNII lookup
91D9GV0Z28Internal UNII lookup
HF539G9L3QInternal UNII lookup
5405K23S50Internal UNII lookup
4QQN74LH4OInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5bf53a99-b3b0-48bb-828b-39cd0839840aAvailable on FDA.report

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69727-0003-1Ultra Advantage30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69727-0003ULTRA ADVANTAGE (ABROTANUM (ARTEMISIA ABROTANUM), ANACARDIUM ORIENTALE, FUCUS VESICULOSUS, HELLEBORUS NIGER, HYPOTHALAMUS SUIS, LYCOPODIUM CLAVATUM, THYMOLUM, THYMUS SERPYLLUM, THYROIDINUM (BOVINE), GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, PANCREAS SUIS, CINCHONA OFFICINALIS, NICOTINAMIDUM, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, MAGNESIA PHOSPHORICA, SOLIDAGO VIRGAUREA, GRAPHITES) LIQUID [ELTTAC INC DBA SWL]1Current NDC, Legacy NDC, 1 package rows20190913_5bf53a99-b3b0-48bb-828b-39cd0839840a.zip

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
Ultra AdvantageABROTANUM (ARTEMISIA ABROTANUM), ANACARDIUM ORIENTALE, FUCUS VESICULOSUS, HELLEBORUS NIGER, HYPOTHALAMUS SUIS, LYCOPODIUM CLAVATUM, THYMOLUM, THYMUS SERPYLLUM, THYROIDINUM (BOVINE), GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, PANCREAS SUIS, CINCHONA OFFICINALIS, NICOTINAMIDUM, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, MAGNESIA PHOSPHORICA, SOLIDAGO VIRGAUREA, GRAPHITESELTTAC Inc DBA SWL5bf53a99-b3b0-48bb-828b-39cd0839840a2025-06-03WarningsExact identifier
ndc (product): 69727-0003

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69727-0003-16972700030130 mL in 1 BOTTLE, DROPPER (69727-0003-1) 30 ml2019-09-030000-00-00NoNoCurrent