Bestmade Natural Products BM203

Manufacturer
Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date
2025-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:22

Label at a glance#

ProductBestmade Natural Products BM203
Active ingredientPSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE, FORMIC ACID, RANUNCULUS BULBOSUS WHOLE, BLACK COHOSH, RHODODENDRON TOMENTOSUM LEAFY TWIG, CITRULLUS COLOCYNTHIS FRUIT PULP
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

How to Use

Mix with half a cup of water 3-4 times per day. Ages 12 or older, 10 drops. Ages 12-2, 5 drops. Ages 2 and under, consult your Doctor.

INACTIVE INGREDIENT SECTION

Inactive:

Alcohol Base to Preserve Product

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS

Cimicifuga D100+100C 0.10mL each (HPUS), Colocynthis D100+100C 0.10mL each (HPUS), Formic acid D100+100C 0.10mL each (HPUS), Gnaphalium D100+100C 0.10mL each (HPUS), Ledum pal D100+100C 0.10mL each (HPUS) Ranunculus bulb D100+100C 0.10mL each (HPUS)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings and Storage:


Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms.

Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place


*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE NOT FDA EVALUATED.
This product is not intended to diagnose, treat, cure, or prevent any disease.

WARNINGS SECTION

Warnings and Storage:


Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms.

Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place


*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE NOT FDA EVALUATED.
This product is not intended to diagnose, treat, cure, or prevent any disease.

INDICATIONS & USAGE SECTION

Uses
Temporarily relieves occasional nerve aches and discomfort, lower backaches, sore legs, shooting discomfort, numbness, and weakness of the lower leg muscles.*

OTC - PURPOSE SECTION

Uses
Temporarily relieves occasional nerve aches and discomfort, lower backaches, sore legs, shooting discomfort, numbness, and weakness of the lower leg muscles.*

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Entire package label

BM203 Liquid.jpgBM203 Liquid.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82969-2203-1Bestmade Natural Products BM20330 [hp_C] in 1 BOTTLE, GLASSLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82969-2203BESTMADE NATURAL PRODUCTS BM203 (CIMICIFUGA, COLOCYNTHIS, FORMIC ACID, GNAPHALIUM, LEDUM PAL, RANUNCULUS BULB) LIQUID [BESTMADE NATURAL PRODUCTS]1Current NDC, 1 package rows20250417_2ef994dc-ddea-afa7-e063-6394a90affd2.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-220382969-2203-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Bestmade Natural Products BM203CIMICIFUGA, COLOCYNTHIS, FORMIC ACID, GNAPHALIUM, LEDUM PAL, RANUNCULUS BULBBestmade Natural Products2ef994dc-ddea-afa7-e063-6394a90affd22025-02-25WarningsExact identifier
ndc (package): 82969-2203-1
ndc (product): 82969-2203
ndc11 (package): 82969220301
spl id: 2ef994dc-ddeb-afa7-e063-6394a90affd2
spl set id: 2ef994dc-ddea-afa7-e063-6394a90affd2

Reported adverse events (FAERS/openFDA)#

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