Label: CIZAR FIRST CALMING TONER- glycerin liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 71128-040-01, 71128-040-02 - Packager: Tissuegene,inc
- 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 17, 2018
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: Water, Alcohol Denat., Pentylene Glycol, 1,2-Hexanediol, Saccharum Officinarum (Sugarcane) Extract, Chondrus Crispus Extract, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Citric Acid, Octyldodeceth-16, Panthenol, Xanthan Gum, Arginine, Lavandula Angustifolia (Lavender) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Disodium EDTA, Zinc Oxide, Butylene Glycol, Adonis Amurensis Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Gentiana Scabra Root Extract, Viola Mandshurica Flower Extract
- PURPOSE
-
WARNINGS
Warnings:
For external use only When using this product do not get into eyes, Stop use and ask a doctor if rash occurs Do not use on - deep puncture wounds - animal bites - serious burns
Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep Out of Reach of Children
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CIZAR FIRST CALMING TONER
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71128-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 4.8 g in 120 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Pentylene Glycol (UNII: 50C1307PZG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71128-040-02 1 in 1 CARTON 06/01/2017 1 NDC:71128-040-01 120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2017 Labeler - Tissuegene,inc (694860183) Registrant - Tissuegene,inc (694860183) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(71128-040)
