DIO WHITENING is a Dental Paste, Dentifrice in the Human Otc Drug category. It is labeled and distributed by Dio Corporation. The primary component is Silicon Dioxide; .alpha.-tocopherol Acetate; Hydrogen Peroxide.
Product ID | 75902-4001_50e23c08-7305-6d1a-e054-00144ff8d46c |
NDC | 75902-4001 |
Product Type | Human Otc Drug |
Proprietary Name | DIO WHITENING |
Generic Name | Sodium Fluoride |
Dosage Form | Paste, Dentifrice |
Route of Administration | DENTAL |
Marketing Start Date | 2015-01-22 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Dio Corporation |
Substance Name | SILICON DIOXIDE; .ALPHA.-TOCOPHEROL ACETATE; HYDROGEN PEROXIDE |
Active Ingredient Strength | 7 g/100g; g/100g; g/100g |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2015-01-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-01-22 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
SILICON DIOXIDE | 7 g/100g |
SPL SET ID: | 1b5a5f59-fa6a-4ce6-a360-502fb651eb1a |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
75902-4001 | DIO WHITENING | DIO WHITENING |
0135-0234 | AQUAFRESH | sodium fluoride |
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