Label: DIVINETREE SSAK SHARK KIDS TOOTH- silicon dioxide, alcloxa paste, dentifrice
-
Contains inactivated NDC Code(s)
NDC Code(s): 73494-010-01, 73494-010-02 - Packager: K.biocos
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 4, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive Ingredients:
Glycerin, Sorbitol, Cellulose Gum, Xylitol, Ascorbic Acid, Stevioside, Glycyrrhiza Glabra (Licorice) Root Extract, Salvia Officinalis (Sage) Leaf Extract, Calcium Glycerophosphate, Milk, Lavandula Angustifolia (Lavender) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Calendula Officinalis Flower Extract, Streptococcus Thermophilus Ferment, Chamomilla Recutita (Matricaria) Flower Extract, Chamaecyparis Obtusa Oil, Eucalyptus Globulus Leaf Oil, Flavor, Sodium Cocoyl Glutamate, Sodium Lauroyl Sarcosinate, Water
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DIVINETREE SSAK SHARK KIDS TOOTH
silicon dioxide, alcloxa paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73494-010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6.50 g in 50 g ALCLOXA (UNII: 18B8O9DQA2) (ALLANTOIN - UNII:344S277G0Z) ALCLOXA 0.08 g in 50 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73494-010-02 1 in 1 CARTON 11/01/2019 1 NDC:73494-010-01 50 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/01/2019 Labeler - K.biocos (695640141) Registrant - K.biocos (695640141) Establishment Name Address ID/FEI Business Operations Korea Life Science Co.,ltd 694914835 manufacture(73494-010)