OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Sodium Fluoride 0.21%
CLOSE UP TRAVEL
- Manufacturer
- JHS SVENDGAARD LABORATORIES LIMITED
- Effective date
- 2022-08-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:50:22
Label at a glance#
ProductCLOSE UP TRAVEL
Active ingredientSODIUM FLUORIDE
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Purpose:
Anticavity
INDICATIONS & USAGE SECTION
Uses:
Aids in the prevention of dental cavities
WARNINGS SECTION
Warnings:
If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children under 6 years of age
DOSAGE & ADMINISTRATION SECTION
Directions:
- Do not swallow.
Adults and children 2 years and older:
Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.
Children under 6 Years of Age
Use only a pea-sized amount and supervise children's brushing and rinsing to minimize swallowing.
Children under 2 years of age:
Ask a dentist or physician
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Sorbitor, Water, Silica, Sodium Lauryl Suphate, PEG-32, Titanium Dioxide, Flavor, Cellulose Gum, Cocamidopropyl Betaine, Sodium Saccharin, Zinc Sulfate, Sodium Hydroxide, D&C Red 33, FD&C Red 40, Synthetic Fluorphlogopite, Melaleuca Alternifolia (Tea Tree Extract), Eucalyptus Globulus (Eucalyptus Extract), Eugenol
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72025-004-01 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-7287-198a-e063-dbdaa90aec3e | 72025-004 |
| 72025-004-02 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-7287-198a-e063-dbdaa90aec3e | 72025-004 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72025-004-01 | CLOSE UP TRAVEL | 79 g in 1 TUBE | PASTE, DENTIFRICE | 79 | 2 | |
| 72025-004-02 | CLOSE UP TRAVEL | 24 g in 1 TUBE | PASTE, DENTIFRICE | 24 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CLOSE UP TRAVEL
- SODIUM FLUORIDE
- WATER
- SORBITOL
- SODIUM LAURYL SULFATE
- ALPHA CELLULOSE
- SODIUM SILICATE
- TITANIUM DIOXIDE
- SACCHARIN SODIUM
- PEG-32 LAURATE
- COCAMIDOPROPYL BETAINE
- ZINC SULFATE
- SODIUM HYDROXIDE
- D&C RED NO. 33
- FD&C RED NO. 40
- MELALEUCA ALTERNIFOLIA WHOLE
- EUCALYPTUS GLOBULUS WHOLE
- EUGENOL
- FLUORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72025-004 | 72025-004-01, 72025-004-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| e5ec21b7-c798-b8af-e053-2995a90a870e | c9a4c874-a35e-4221-a627-6421d5a70f26 | 2022-08-10 | Warnings | e5ec21b7-c798-b8af-e053-2995a90a870e c9a4c874-a35e-4221-a627-6421d5a70f26 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.