BMNP-LABEL NATRUM SALICYLICUM 30C

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-10-13 04:02:12

Label at a glance#

ProductBMNP NATRUM SALICYLICUM
Active ingredientSODIUM SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Keep out of reach of children.

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

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

If you have severe symptoms, consult a doctor before use.

DOSAGE & ADMINISTRATION SECTION

Use as directed.

Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 3: consult your doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

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

If you have severe symptoms, consult a doctor before use.

INDICATIONS & USAGE SECTION

Helps temporarily relieve: ear sensitivity, poor balance, ringing or buzzing sensations, head discomfort

OTC - PURPOSE SECTION

Natrum Salicylicum 30C (HPUS)......sensitivity and irritation in the head or ears, head discomfort, ringing or buzzing sensations

"HPUS" is the Homeopathic Pharmacopoeia of the United States.

OTC - ACTIVE INGREDIENT SECTION

NATRUM SALICYLICUM 30C

INACTIVE INGREDIENT SECTION

Sucrose, PVP K 30, Magnesium Stearate, Aerosil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 2

Nat Sal 30CNat Sal 30C

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codefastremedypicker.com/-_Nat Sal 30C.jpg

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-531382969-5313-1, 82969-5313-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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