Insomnia

Manufacturer
Natural Health Supply
Effective date
2019-04-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:11:16

Label at a glance#

ProductInsomnia
Active ingredientPOTASSIUM CATION
Label structure8 sections

Dosage and administration

Take at onset of symptoms.  Repeat every 2 hours or as needed until relieved.  If condition persists or worsens discontinue use and consult a practitioner. Adults: dissolve 5-10 pellets in 1 oz. of filtered water or take dry by mouth.  Children and infants: 1-5 pellets.

Label contents#

Full prescribing information#

Indications

INDICATIONS & USAGE SECTION

Indications: To be used for acute self-limiting conditions according to standard homeopathic indications

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

POTASSIUM CATION

Directions

DOSAGE & ADMINISTRATION SECTION

Take at onset of symptoms.  Repeat every 2 hours or as needed until relieved.  If condition persists or worsens discontinue use and consult a practitioner.

Adults: dissolve 5-10 pellets in 1 oz. of filtered water or take dry by mouth.  Children and infants: 1-5 pellets.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep these and all medications out of the reach of children.

Warning

WARNINGS SECTION

If pregnant or nursing, consult a practitioner before using.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients - Lactose, Sucrose

Purpose

OTC - PURPOSE SECTION

Purpose: Insomnia

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est. No. 1724217

Natural Health Supply

505-474-9175

Homeopathic Medicated Pellets

Do not use if clear bottle seal is broken

POTASSIUM CATION 30c

Insomnia

Lot #__________________

Insomnia Label 3Insomnia Label 3

res

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
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64117-151-012024-01-30C16284748780-11030e365-3e79-111a-e063-dadaa90a10e2f05f715a-4fa4-492a-be9c-fcc9d9c062d7
64117-151-022024-01-30C16284748780-11030e365-3e79-111a-e063-dadaa90a10e2f05f715a-4fa4-492a-be9c-fcc9d9c062d7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64117-151-01Insomnia1.875 mL in 1 BOTTLE, GLASSPELLET1.8752
64117-151-02Insomnia7.5 mL in 1 BOTTLE, GLASSPELLET7.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64117-151INSOMNIA (POTASSIUM CATION) PELLET [NATURAL HEALTH SUPPLY]2Legacy NDC, 2 package rows20190409_f05f715a-4fa4-492a-be9c-fcc9d9c062d7.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64117-15164117-151-01, 64117-151-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM CATION295O53K152ACTIB
LACTOSEJ2B2A4N98GIACT
SUCROSEC151H8M554IACT

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
9b7c09da-04d4-42eb-b28d-8e33cd89542ef05f715a-4fa4-492a-be9c-fcc9d9c062d72019-04-08WarningsExact identifier
spl id: 9b7c09da-04d4-42eb-b28d-8e33cd89542e
spl set id: f05f715a-4fa4-492a-be9c-fcc9d9c062d7

Reported adverse events (FAERS/openFDA)#

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