RENAFORCE

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2026-03-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:37:53

Label at a glance#

ProductRENAFORCE
Active ingredientBERBERIS VULGARIS ROOT BARK, ECHINACEA ANGUSTIFOLIA WHOLE, PROTORTONIA CACTI, POTASSIUM CHLORIDE, LYCOPODIUM CLAVATUM SPORE, NITRIC ACID
Label structure9 sections

Indications and uses

For temporary relief of urine that's scanty, dark, offensive; pain in the back, sensation as if some urine remained after urinating and pain in the  thighs and loins on urinating.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

• 10 drops orally, 3 times a day or as directed by a health care professional. • Consult a health care professional for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Berberis Vulgaris 3X, Coccus Cacti 12X, Echinacea (Angustifolia) 3X, Kali Muriaticum 12X, Lycopodium Clavatum 12X, Nitricum Acidum 12X.

PURPOSE:

OTC - PURPOSE SECTION

Berberis Vulgaris – liver support,** Coccus Cacti – spasmodic pain in kidneys,** Echinacea (Angustifolia) – pain or burning,** Kali Muriaticum - headache,** Lycopodium Clavatum – burning with urination,** Nitricum Acidum – fever**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

USES:

INDICATIONS & USAGE SECTION

For temporary relief of urine that's scanty, dark, offensive; pain in the back, sensation as if some urine remained after urinating and pain in the  thighs and loins on urinating.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care professional before use

Keep out of reach of children. In case of overdose, get medical attention or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

• 10 drops orally, 3 times a day or as directed by a health care professional.

• Consult a health care professional for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com

1-800-288-9525

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

RENAFORCE

HOMEOPATHIC

1 fl. oz. (30 mL)

RENAFORCERENAFORCE

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130210184341220GTIN-13: 0210184341220
EAN-13: 0210184341220
GTIN-12: 210184341220
UPC-A: 210184341220
GTIN storage (14 digits): 00210184341220
BANI61 Renaforce 11-11-25.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
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290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
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ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0340-1RENAFORCE30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BERBERIS VULGARIS ROOT BARKACTIVE INGREDIENT1TH8Q20J0U1
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US81
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
NITRIC ACIDACTIVE INGREDIENT411VRN1TV41
POTASSIUM CHLORIDEACTIVE INGREDIENT660YQ98I101
PROTORTONIA CACTIACTIVE INGREDIENTLZB7TFX1LT1
BERBERIS VULGARIS ROOT BARKACTIVE MOIETY1TH8Q20J0U1
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US81
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
NITRIC ACIDACTIVE MOIETY411VRN1TV41
POTASSIUM CATIONACTIVE MOIETY295O53K1521
PROTORTONIA CACTIACTIVE MOIETYLZB7TFX1LT1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-034043857-0340-1

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
RENAFORCEBERBERIS VULGARIS, ECHINACEA (ANGUSTIFOLIA), COCCUS CACTI, KALI MURIATICUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUMBioActive Nutritional, Inc.804b7055-e1e6-448d-8257-c562b971f4372026-03-09WarningsExact identifier
ndc (package): 43857-0340-1
ndc (product): 43857-0340
ndc11 (package): 43857034001
spl id: 5b590753-cd51-487e-ad66-90558a3f03fa
spl set id: 804b7055-e1e6-448d-8257-c562b971f437

Reported adverse events (FAERS/openFDA)#

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