Label: GLIZIGEN SKIN PROTECTANT- glycerin spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 64539-018-01 - Packager: Catalysis, SL
- 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 March 22, 2018
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
- ASK DOCTOR
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- QUESTIONS
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PURPOSE
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GLIZIGEN SKIN PROTECTANT
glycerin sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64539-018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength POLYSORBATE 80 (UNII: 6OZP39ZG8H) 0.8 mg in 1 mL SODIUM BENZOATE (UNII: OJ245FE5EU) 0.1 mg in 1 mL POTASSIUM SORBATE (UNII: 1VPU26JZZ4) 0.1 mg in 1 mL WATER (UNII: 059QF0KO0R) 100 mg in 1 mL PROPANEDIOL (UNII: 5965N8W85T) 50 mg in 1 mL TEA LEAF (UNII: GH42T47V24) 0.1 mg in 1 mL GLYCYRRHIZIN (UNII: 6FO62043WK) 0.1 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64539-018-01 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/22/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 03/22/2018 Labeler - Catalysis, SL (862795119) Registrant - Catalysis, SL (862795119) Establishment Name Address ID/FEI Business Operations Catalysis, SL 862795119 manufacture(64539-018)