HKI

Manufacturer
Seroyal USA | SAN'UP
Effective date
2023-01-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:20:00

Label at a glance#

ProductHKI
Active ingredientATROPINE SULFATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CITRULLUS COLOCYNTHIS FRUIT PULP, LYCOPODIUM CLAVATUM SPORE, ORYCTOLAGUS CUNICULUS KIDNEY, SARSAPARILLA, CALCIUM HEXAFLUOROSILICATE, BENZOIC ACID, PROTORTONIA CACTI, LITHIUM CARBONATE, RUBIA TINCTORUM ROOT, URTICA URENS, BERBERIS VULGARIS ROOT BARK
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each drop contains:

Atropinum sulphuricum 6X

Benzoicum acidum 6X
Berberis vulgaris (Barberry) Bark 5X
Calcarea carbonica 12X
Colocynthis (Bitter apple) Dried fruit 6X

Coccus cacti (Cochineal) 5X

Lapis albus (Gastein rock) 12CH

Lithium carbonicum 6X
Lycopodium clavatum (Clubmoss) Spores 5X
Oryctolagus cuniculus (Rabbit) Kidney 10X

Rubia tinctorum (Madder) Root 4X
Sarsaparilla Root 1X

Urtica urens (Dwarf Nettle) Aerial parts 1X

OTC - PURPOSE SECTION

Uses

Helps promote and maintain healthy kidney and urinary tract functions.

WARNINGS SECTION

Warnings
Stop use and ask a doctor if symptoms persist or worsen.
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

Contains Shellfish (oyster)

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients

Ethanol (beet), purified water

OTHER SAFETY INFORMATION

Other information

Store in a cool, dry place.

Contents may not fill package in order to accommodate required labeling. Please rely on stated quantity.

OTC - DO NOT USE SECTION

Use only if safety seal is intact.

DOSAGE & ADMINISTRATION SECTION

Directions

To be taken 20 minutes away from food.

Place drops directly under the tongue or into ¼ oz of water.

Adults and adolescents (12 years and older): Take 10 drops two to three times daily or as recommended by your healthcare practitioner.

Children (under 12 years): Take under the direction of your healthcare practitioner.

INDICATIONS & USAGE SECTION

Uses

Helps promote and maintain healthy kidney and urinary tract functions.

Directions

To be taken 20 minutes away from food.

Place drops directly under the tongue or into ¼ oz of water.

Adults and adolescents (12 years and older): Take 10 drops two to three times daily or as recommended by your healthcare practitioner.

Children (under 12 years): Take under the direction of your healthcare practitioner.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Genestra Brands

NDC 62106-0625-0

HKI

HOMEOPATHIC PREPARATION

To help promote and maintain
kidney and urinary tract health.

Contains 48% Alcohol

1 fl oz (30 mL)

HKI PDPHKI PDPHKI warningsHKI warnings

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c78bd43-efb4-4aeb-b7d8-eff1532f7822Product name420250801
41231c1e-8789-4da7-ac52-77fa90a85bf5Product name220250304
e77ab9a2-80cf-4832-bff0-469bbc7cbcd0Product name220250214
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
5f84b7a7-523a-f042-dffb-1dadcd9b2407Product name420240110
0cbc6fb2-78c0-4b88-98f0-a4cc76ff95caProduct name120230719
04cd5dc0-102f-46cb-8dbc-ca38dd2628d0Product name320230317
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dfd25202-b8d2-4628-9213-f3e0f9eafce5Product name420210513
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205
4199bf9b-4718-828a-6dd6-ac2fbbd61687Product name120140508
4edd8af5-cea7-ae42-8023-e91c5335db1dProduct name120140508
d3908afb-7784-440f-c406-88294732d36aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-0625-0HKI30 mL in 1 BOTTLE, GLASSLIQUID305
62106-0625-0HKI1 in 1 CARTONLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-0625HKI (ATROPINUM SULPHURICUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, CALCAREA CARBONICA, COLOCYNTHIS, COCCUS CACTI, LAPIS ALBUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, ORYCTOLAGUS CUNICULUS KIDNEY, RUBIA TINCTORUM, SARSAPARILLA, URTICA URENS) LIQUID [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20230201_26e048f5-8e87-51e6-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-062562106-0625-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

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
HKIATROPINUM SULPHURICUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, CALCAREA CARBONICA, COLOCYNTHIS, COCCUS CACTI, LAPIS ALBUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, ORYCTOLAGUS CUNICULUS KIDNEY, RUBIA TINCTORUM, SARSAPARILLA, URTICA URENSSeroyal USA26e048f5-8e87-51e6-e054-00144ff88e882023-01-31WarningsExact identifier
ndc (package): 62106-0625-0
ndc (product): 62106-0625
ndc11 (package): 62106062500
spl id: f38e873c-cc3c-f701-e053-2a95a90af213
spl set id: 26e048f5-8e87-51e6-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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