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
Product NDC
53045-0200-00 53045-0200-17 53045-0200-08
Package NDC
53045-200-17 53045-200-08

Drug Facts

Composition & Profile

Inactive Ingredients
Citric Acid FD & C Red No. 40 (C.I. 16035) Flavor 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 53045-0200-00
All Product Codes
53045-0200-00 53045-0200-17 53045-0200-08
UPC
0353045000222
UNII
8ZYQ1474W7
SPL Set IDs
503ca71a-f50c-4406-b925-5b6ac36a9212
Packaging

20200514_200_08_RevB 20200514_200_17_RevB

Package Descriptions
  • 20200514_200_08_RevB 20200514_200_17_RevB
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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