WHP Be gone Teething

Manufacturer
Washington Homeopathic Products
Effective date
2014-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:48

Label at a glance#

ProductWHP Be gone Teething TM
Active ingredientTRIBASIC CALCIUM PHOSPHATE, MATRICARIA CHAMOMILLA, ARABICA COFFEE BEAN
Label structure8 sections

Indications and uses

To relieve the symptoms of irritability restlessness, backwardness in getting teeth and other symptoms associated with difficult dentition.

Dosage and administration

3 to 5 pills every 3 hours for 2 days. Then 3 to 5 pills morning and night for 2 weeks.  Repeat as necessary.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

CALC PHOS

CHAMOMILLA

COFFEA CRUDA

USES

OTC - PURPOSE SECTION

To relieve the symptoms of irritability restlessness, backwardness in getting teeth and other symptoms associated with difficult dentition.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

AS with all medications, keep out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

Calc phos 6c –troubled teething*

Chamomilla 6c –distressed teething*

Coffea cruda 6c –sensitive teething*

■ Irritability ■ Restlessness ■ Sleeplessness

*These statements have not been reviewed by the Food and Drug Administration.

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist or recur, discontinue use. If pregnant or nursing a baby, consult a licensed practitioner before using this product.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

3 to 5 pills every 3 hours for 2 days. Then 3 to 5 pills morning and night for 2 weeks. Repeat as necessary.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose Pills

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

image of boximage of box

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
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0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68428-862-292025-01-30C16284748780-12cef2736-5a3a-d83d-e063-dadaa90ab31fDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-862-14WHP Be gone TeethingTM12000 in 1 BOTTLE, PLASTICPELLET120001
68428-862-29WHP Be gone TeethingTM1 in 1 PACKAGEPELLET11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-862WHP BE GONE TEETHING TM (TRIBASIC CALCIUM PHOSPHATE - MATRICARIA CHAMOMILLA - ARABICA COFFEE BEAN) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]1Legacy NDC, 2 package rows20170609_73ba18f4-a04f-4346-b5bd-d439697938e8.zip

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
68428-86268428-862-14, 68428-862-29

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

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
733afb95-1344-4adf-a336-bff36baaebcc73ba18f4-a04f-4346-b5bd-d439697938e82014-05-08WarningsExact identifier
spl id: 733afb95-1344-4adf-a336-bff36baaebcc
spl set id: 73ba18f4-a04f-4346-b5bd-d439697938e8

Reported adverse events (FAERS/openFDA)#

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