SPL UNCLASSIFIED SECTION
Drug Facts
Auraglow Whitening
- Manufacturer
- Auraglow LLC
- Effective date
- 2025-10-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:40:25
Label at a glance#
ProductAuraglow Whitening
Active ingredientSODIUM FLUORIDE
Label structure9 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Sodium fluoride 0.23%
(0.15% w/v fluoride ion)
OTC - PURPOSE SECTION
Purpose Anticavity
INDICATIONS & USAGE SECTION
Use Helps protect against cavities
WARNINGS SECTION
Warnings
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children under 6 years of age.
If more than used for brushing is accidentally swallowed, get
medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
• Adults and children 2 years of age and older:
Brush teeth thouroughly, preferably after each meal or
at least twice a day, or as directed by a dentist or doctor.
• Instruct children under 6 years of age in good brushing
and rinsing habits (to minimize swallowing). • Supervise
children as necessary until capable of using without supervision.
• Children under 2 years of age: Consult a dentist or doctor.
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Water, Sorbitol, Hydrated Silica, Glycerin,
Xylitol, Natural Wintergreen Flavor, Cellulose
Gum, Sodium Lauroyl Sarcosinate, Sodium
Saccharin, Carrargeenan, Titanium Dioxide,
Hydrogen Peroxide, Menthol
Package Labeling
----------------------------------
Auraglow
Whitening
Toothpaste
Removes surface stains
and helps prevent cavities.
WINTERGREEN
FLUORIDE TOOTHPASTE
NET WT 4.0 OZ (113G)
Distr. by Auraglow LLC, Stamford, CT 06901
CARTON
TUBE
res
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5eb9f24b-9328-475e-af0a-18021935eb6a | Product name | 1 | 20180220 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81740-003-03 | Auraglow Whitening | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | 1 | |
| 81740-003-03 | Auraglow Whitening | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | 1 |
Products#
Every source-derived product name is available through these pages.
- Auraglow Whitening
- SODIUM FLUORIDE
- FLUORIDE ION
- WATER
- SORBITOL
- HYDRATED SILICA
- GLYCERIN
- XYLITOL
- CELLULOSE GUM
- SODIUM LAUROYL SARCOSINATE
- SODIUM SACCHARIN
- CARRAGEENAN
- TITANIUM DIOXIDE
- HYDROGEN PEROXIDE
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81740-003 | 81740-003-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM FLUORIDE | 8ZYQ1474W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SORBITOL | 506T60A25R | IACT |
| HYDRATED SILICA | Y6O7T4G8P9 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| XYLITOL | VCQ006KQ1E | IACT |
| CELLULOSE GUM | K679OBS311 | IACT |
| SODIUM LAUROYL SARCOSINATE | 632GS99618 | IACT |
| SODIUM SACCHARIN | SB8ZUX40TY | IACT |
| CARRAGEENAN | 5C69YCD2YJ | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| MENTHOL | L7T10EIP3A | IACT |
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 |
|---|---|---|---|---|---|---|
| Auraglow Whitening | SODIUM FLUORIDE | Auraglow LLC | 9d45e436-92f6-4a9e-9b82-329847dca9ba | 2025-10-22 | Warnings | 81740-003-03 81740-003 81740000303 3f72b20e-32ad-468c-a67b-ff438c3a8396 9d45e436-92f6-4a9e-9b82-329847dca9ba |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.