AdoptaPlatoon

Manufacturer: Yangzhou ONE & ONLY Personal Care Products Co., LTD
Effective date: 2025-03-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:57:38

Label at a glance#

ProductAdoptaPlatoon

Active ingredientSODIUM FLUORIDE

Label structure6 sections

Indications and uses

Help protect against dental cavities.

Dosage and administration

Adult and children six years of age or older: Brush teeth thoroughly, preferrably after each meal or at least twice a day, or as directed by a dentist or a physician. Children 2-6: Use only a pea sized amount and supervise children's brushing and rinsing to minimize swallowing. Children under 2: Ask a dentist or physician

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.22%(0.1 w/v Fluoride ion)

Purpose

OTC - PURPOSE SECTION

anticavity

Uses

INDICATIONS & USAGE SECTION

Help protect against dental cavities.

Warnings

WARNINGS SECTION

Keep out of the reach of children under 6 years of age. If more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Adult and children six years of age or older:

Brush teeth thoroughly, preferrably after each meal or at least twice a day, or as directed by a dentist or a physician.

Children 2-6:

Use only a pea sized amount and supervise children's brushing and rinsing to minimize swallowing.

Children under 2:

Ask a dentist or physician

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Sorbitol, Silica,Methyl Paraben Sodium, Propyl Paraben Sodium, Sodium Saccharin, Flavor, Water, SCMC, Sodium Lauryl Sulfate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
245598	sodium fluoride 0.22 % Toothpaste	PSN	1
245598	sodium fluoride 0.0022 MG/MG Toothpaste	SCD	1
245598	sodium fluoride 0.22 % (fluoride 0.1 % ) Toothpaste	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
85162-004-01	AdoptaPlatoon	10 mL in 1 TUBE	PASTE, DENTIFRICE	10	1
85162-004-02	AdoptaPlatoon	30 in 1 BOX	PASTE, DENTIFRICE	30	1
85162-004-02	AdoptaPlatoon	10 mL in 1 TUBE	PASTE, DENTIFRICE	10	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
85162-004	ADOPTAPLATOON (SODIUM FLUORIDE) PASTE, DENTIFRICE [YANGZHOU ONE & ONLY PERSONAL CARE PRODUCTS CO., LTD]	1	Current NDC, 3 package rows	20250323_c1592b56-cf3d-4a4d-be84-e40eb3f1456e.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

AdoptaPlatoon
Sodium Fluoride
SACCHARIN SODIUM
SORBITOL
METHYLPARABEN SODIUM
HYDRATED SILICA
SODIUM LAURYL SULFATE
PROPYLPARABEN SODIUM
WATER
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85162-004	85162-004-02, 85162-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SACCHARIN SODIUM	SB8ZUX40TY	IACT
SORBITOL	506T60A25R	IACT
METHYLPARABEN SODIUM	CR6K9C2NHK	IACT
HYDRATED SILICA	Y6O7T4G8P9	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
PROPYLPARABEN SODIUM	625NNB0G9N	IACT
WATER	059QF0KO0R	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AdoptaPlatoon	SODIUM FLUORIDE	Yangzhou ONE & ONLY Personal Care Products Co., LTD	c1592b56-cf3d-4a4d-be84-e40eb3f1456e	2025-03-21	Warnings	Exact identifier ndc (package): 85162-004-01 ndc (package): 85162-004-02 ndc (product): 85162-004 ndc11 (package): 85162000401 ndc11 (package): 85162000402 spl id: 30d37581-1223-ec92-e063-6294a90ab425 spl set id: c1592b56-cf3d-4a4d-be84-e40eb3f1456e

Reported adverse events (FAERS/openFDA)#

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