Label: CLEAR QQ- sodium fluoride paste, dentifrice
-
Contains inactivated NDC Code(s)
NDC Code(s): 70164-010-01 - Packager: YOURMG. CO. LTD
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 23, 2015
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive Ingredients: D-Sorbitol 70%, Allantoin, Sodium Saccharine, Mono Sodium Glutamate, Sodium Benzoate, Allantoin Chlor Hydroxy Aluminium, Amino Capronic Acid, Conc Glycerine, Sodium Bicarbonate, Citric Acid, Butylene Glycol, Purified Water, Centella Asiatica Extract, Scutellaria Baicalensis Root Extract, Polygonum Cuspidatum Root Extract, Glycyrryhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Rose marinus Officinalis (Rosemary)Leaf Extract, Chamomilla Recutita (Matricaria)Flower Extract, Sodium Carboxy Methyl Cellulose, Ethanol, L- Mentol, Apple mint Flavor
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
INDICATIONS & USAGE
Directions: 1) Adults and children 2 years of age and older: Brush teeth throughly preferably after each meal or at least twice a day or as directed by a dentist or doctor. 2) Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established. 3) Children under 2 years: Consult a dentist or doctor
-
DOSAGE & ADMINISTRATION
Directions: 1) Adults and children 2 years of age and older: Brush teeth throughly preferably after each meal or at least twice a day or as directed by a dentist or doctor. 2) Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established. 3) Children under 2 years: Consult a dentist or doctor
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEAR QQ
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70164-010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Fluoride (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.75 g in 150 g Inactive Ingredients Ingredient Name Strength Allantoin (UNII: 344S277G0Z) Sodium Bicarbonate (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70164-010-01 150 g in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 09/01/2015 Labeler - YOURMG. CO. LTD (687578133) Registrant - YOURMG. CO. LTD (687578133) Establishment Name Address ID/FEI Business Operations YOURMG. CO. LTD 687578133 manufacture(70164-010)
