ME MOTHER EARTH

Manufacturer
A PLUS MERCHANDISE LLC
Effective date
2025-11-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:41

Label at a glance#

ProductME MOTHER EARTH
Active ingredientSODIUM FLUORIDE
Label structure9 sections

Dosage and administration

Adults and children 6 years and older: Chew. Brush. Smile. Save the planet. Use after each meal or at least twice daily. Do not swallow the tablet. Supervise children under the age of 6.

Storage and handling

Store in a cool dry place. Pour into our refillable glass jar or any sealed, repurposed container of your choice. Protect from excessive moisture. Keep away from pets.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.32% (1450 ppm fluoride ion) — Anticavity

Purpose

OTC - PURPOSE SECTION

Anti-cavity

Use

INDICATIONS & USAGE SECTION

Helps prevent tooth decay caused by cavities

Warnings

WARNINGS SECTION

  • If irritation or sensitivity occurs, stop use and consult a dentist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 6 years and older: Chew. Brush. Smile. Save the planet. Use after each meal or at least twice daily. Do not swallow the tablet. Supervise children under the age of 6.

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place. Pour into our refillable glass jar or any sealed, repurposed container of your choice. Protect from excessive moisture. Keep away from pets.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Xylitol, Microcrystalline Cellulose, Sorbitol, Calcium Carbonate, Peppermint (Mentha arvensis) Oil Powder, Sodium Cocoyl Isethionate, Silicon Dioxide, Inulin, Acacia Gum, Zinc Oxide, Menthol, Ammonium Glycyrrhizate, Sodium Bicarbonate, Tapioca Starch, Aloe Vera Powder.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelPouch LabelPouch Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeinstagram.com/me.motherearth?igshid=YmMyMTA2M2Y=Jar Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87232-444-11ME MOTHER EARTH65 in 1 JARTABLET, CHEWABLE651
87232-444-12ME MOTHER EARTH195 in 1 POUCHTABLET, CHEWABLE1951

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87232-44487232-444-11, 87232-444-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
ME MOTHER EARTHZERO WASTE TOOTHPASTE TABLETS PEPPERMINTA PLUS MERCHANDISE LLC43d30abc-889a-5377-e063-6294a90ab8042025-11-17WarningsExact identifier
ndc (package): 87232-444-12
ndc (package): 87232-444-11
ndc (product): 87232-444
ndc11 (package): 87232044411
ndc11 (package): 87232044412
spl id: 43d30abc-889b-5377-e063-6294a90ab804
spl set id: 43d30abc-889a-5377-e063-6294a90ab804

Reported adverse events (FAERS/openFDA)#

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