87409-001

Manufacturer
POPONSMILES, LLC | Nanchang White Technology Co.,Ltd.
Effective date
2026-08-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-25 01:03:21

Label at a glance#

ProductPop On Toothpaste.
Active ingredientSODIUM FLUORIDE
Label structure13 sections

Dosage and administration

1. Apply 2 pumps to a soft bristle toothbrush. 2. Gently brush it a circular motion for 2 minutes. 3. Expel excess and rinse mouth after use, do not swallow.

Storage and handling

please keep in dry and cool place

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

1. Apply 2 pumps to a soft bristle toothbrush.
2. Gently brush it a circular motion for 2 minutes.
3. Expel excess and rinse mouth after use, do not swallow.

Other information

STORAGE AND HANDLING SECTION

please keep in dry and cool place

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water、Sorbitol、Hydrated Silica、Xylitol、Glycerin、Aroma(Flavour)、Disodium Phosphate、Sodium Gluconate、Sodium Lauroyl Sarcosinate、Calcium Glycerophosphate、Cellulose Gum、Xanthan Gum、Tetrapotassium Pyrophosphate、Benzyl Alcohol、Caprylyl Glycol、Sucralose、Menthol、Pentylene Glycol、Zinc Lactate、Methyl Diisopropyl Propionamide、Benzoic Acid.

Purpose

OTC - PURPOSE SECTION

Teeth cleaning

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride

Use

INDICATIONS & USAGE SECTION

Those who want to clean and whiten their teeth.

Warnings

WARNINGS SECTION

Product is not intended for use by children. Do not swallow. Do not use in eye area.

Do not use

OTC - DO NOT USE SECTION

Product is not intended for use by children.

When Using

OTC - WHEN USING SECTION

Do not swallow. Do not use in eye area.

Stop Use

OTC - STOP USE SECTION

If there is any discomfort, please stop using.

Ask Doctor

OTC - ASK DOCTOR SECTION

If there is any discomfort, please consult a dentist immediately

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of young children

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

22

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130604670299162GTIN-13: 0604670299162
EAN-13: 0604670299162
GTIN-12: 604670299162
UPC-A: 604670299162
GTIN storage (14 digits): 00604670299162
49e56110-2480-739f-e063-6294a90addfc.jpg, POP ON toothpaste(1).jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87409-00187409-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-07-29daily-update2026-08-12 01:01:24
12026-02-02full-release2026-06-01 01:36:47

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
Pop On Toothpaste.POP ON TOOTHPASTE.POPONSMILES,LLC4a0edab5-ae36-91b5-e063-6294a90aa6852026-08-21WarningsExact identifier
ndc (package): 87409-001-01
ndc (product): 87409-001
ndc11 (package): 87409000101
spl id: 599b55c1-ca64-8983-e063-6394a90a1213
spl set id: 4a0edab5-ae36-91b5-e063-6294a90aa685

Reported adverse events (FAERS/openFDA)#

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