Lachnanthes tinctoria 6C

Manufacturer
Boiron | Boiron, Inc.
Effective date
2026-04-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:38:25

Label at a glance#

ProductLachnanthes tinctoria
Active ingredientLACHNANTHES CAROLINIANA
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Lachnanthes tinctoria 6C HPUS (0.44 mg)

The letters “HPUS” indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Lachnanthes tinctoria 6C HPUS (0.44 mg)……………………Relieves stiff neck with cramping

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves symptoms of neck pain associated with muscle strain such as:

▪ minor pain ▪ stiffness ▪ cramping

OTC - DO NOT USE SECTION

Do not use if you have

  • a fever and headache, and your neck is so stiff that you cannot touch your chin to your chest
  • neck pain caused by a fall, blow, or injury
  • jaw pain or cannot move your arm or hand. These could be signs of a serious condition.

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen, new symptoms occur, or if redness or swelling is present. These could be signs of a serious condition.

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

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

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: 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.

Children under 12 years of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

BoironUSA.com

Info@Boiron.com

1-800-BOIRON-1 (1-800-264-7661)

SPL UNCLASSIFIED SECTION

do not use if glued carton end flaps are open or if pellet dispenser seal is broken

contains 0.25 g of sugar per dose

retain carton for full drug facts

Made in France

Distributed by Boiron Inc.

Newtown Square, PA 19073

NECK PAIN RELIEF*

Minor Pain ▪ Stiffness

Cramps*

3 TUBES

APPROX. 80 PELLETS EACH

TOTAL 240 PELLETS

1 TUBE

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

LabelLabellabellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3033-41Lachnanthes tinctoria6 [hp_C] in 1 TUBEPELLET64
0220-3033-43Lachnanthes tinctoria3 in 1 CARTONPELLET34

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-30330220-3033-41, 0220-3033-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
Lachnanthes tinctoriaLACHNANTHES CAROLINIANABoiron7d763053-0923-a788-e053-2991aa0aa6cf2026-04-27Exact identifier
ndc (package): 0220-3033-43
ndc (package): 0220-3033-41
ndc (product): 0220-3033
ndc11 (package): 00220303341
ndc11 (package): 00220303343
spl id: 50733b85-067e-99c3-e063-6394a90a4244
spl set id: 7d763053-0923-a788-e053-2991aa0aa6cf

Reported adverse events (FAERS/openFDA)#

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