Label: GELYNAQUIN ADVANCED NF- fhj3atl51c powder, for solution
-
Contains inactivated NDC Code(s)
NDC Code(s): 82017-003-01 - Packager: JAQUIN DE FRANCIA S A
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated June 23, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- PURPOSE
- QUESTIONS
- STOP USE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
GELYNAQUIN ADVANCED NF
fhj3atl51c powder, for solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82017-003 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C) (BOVINE TYPE I COLLAGEN - UNII:FHJ3ATL51C) BOVINE TYPE I COLLAGEN 0.1 g in 1 g Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) 0.06 g in 1 g VITAMIN D (UNII: 9VU1KI44GP) 0.0001 g in 1 g TURMERIC (UNII: 856YO1Z64F) 0.01 g in 1 g MAGNESIUM CHLORIDE (UNII: 02F3473H9O) 0.01253 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82017-003-01 24 g in 1 BAG; Type 0: Not a Combination Product 06/21/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/21/2021 Labeler - JAQUIN DE FRANCIA S A (880988964) Registrant - JAQUIN DE FRANCIA S A (880988964) Establishment Name Address ID/FEI Business Operations JAQUIN DE FRANCIA S A 880988964 manufacture(82017-003)
