Ionite APF SODIUM FLUORIDE DHARMA RESEARCH, INC. FDA Approved No description available yet.

IONITE APF

Generic: SODIUM FLUORIDE
Mfr: DHARMA RESEARCH, INC. FDA Rx Only
FunFoxMeds box
Substance Sodium Fluoride
Route
DENTAL ORAL TOPICAL
Product NDC
53045-0205-00 53045-0205-17
Package NDC
53045-205-17

Drug Facts

Composition & Profile

Inactive Ingredients
Citric Acid F D & C Red No. 40 (C.I. 16035) Flavor Hydrofluoric Acid Magnesium Aluminum Silicate Phosphoric Acid Polysorbate 20 Purified Water Sodium Benzoate Sodium Saccharin Sweetness Enhancer Titanium Dioxide Tocopheryl Acetate Xanthan Gum Xylitol.

Identifiers & Packaging

Container Type UNKNOWN
NDC 53045-0205-00
All Product Codes
53045-0205-00 53045-0205-17
UNII
8ZYQ1474W7
SPL Set IDs
ab9b07ad-f6b2-4289-bec4-fec58270dc97
Packaging

205

Package Descriptions
  • 205
Overview

No description available yet.

Dosage & Administration

Not available

Warnings & Precautions
Keep out of the reach of children. Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a Poison Control Center right away. Do not use on patients with an allergy Fluoride. Ionite APF Gel contains artificial color, confirm that no kno.wn patient allergies exist. For professional use only.
Storage & Handling

Store at 59 o - 86 o F (15 o - 30 o C) Protect from freezing Ionite APF Gel is free of gluten, soymilk, egg peanut and free of nut products

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Additional Information

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