Natrum sulphuricum

Manufacturer
Boiron | Boiron, Inc.
Effective date
2023-04-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:20:50

Key Label Information#

Active Ingredients And Purpose

OTC - ACTIVE INGREDIENT SECTION

Natrum sulphuricum 30C (**contains 0.443 mg of the active ingredient per pellet)

Uses

INDICATIONS & USAGE SECTION

Bronchial irritation worsened by humidity*

Warnings

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Directions And Dosage

DOSAGE & ADMINISTRATION SECTION

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Other Label Information

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

1-800-BOIRON-1 (1-800-264-7661), BoironUSA.com Info@boiron.com Distributed by Boiron, Inc. Newtown Square, PA 19073

Label Images#

NATSUL30C
NATSUL30C
2ND PANEL
2ND PANEL
3RD PANEL
3RD PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3639-412023-04-11C16284748780-1f386c649-a6a5-0266-e053-dadaa90a7c1aNatrum sulphuricum 30C
0220-3639-412023-01-30C16284748780-1f386c649-a6a5-0266-e053-dadaa90a7c1aNatrum sulphuricum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3639-41Natrum sulphuricum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3639NATRUM SULPHURICUM (SODIUM SULFATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230412_8655cd7d-aa97-ec6f-e053-2a91aa0a33db.zip

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-36390220-3639-41

Ingredients#

Complete SPL Sections#

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Natrum sulphuricum 30C (**contains 0.443 mg of the active ingredient per pellet)

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTION

Bronchial irritation worsened by humidity*

OTC - STOP USE SECTION

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen

OTC - PREGNANCY OR BREAST FEEDING SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Do not use if pellet dispenser seal is broken. Contains approx 80 pellets. How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue. *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED. *C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

lactose, sucrose

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

OTC - QUESTIONS SECTION

OTC - QUESTIONS SECTION

1-800-BOIRON-1 (1-800-264-7661), BoironUSA.com Info@boiron.com Distributed by Boiron, Inc. Newtown Square, PA 19073

Source Document#

Source XML