Label: ARNICA MONTANA NARTEX- arnica montana, hamamelis virginiana cream
- NDC Code(s): 34666-001-10
- Packager: NARTEX LABORATORIOS HOMEOPATICOS SA DE CV
- 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 December 26, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses:
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
DESCRIPTION
Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States, and are therefore non-toxic and have no known side effects.
Product claims are based on Homeopathic Materia Medica. This product has not been clinically tested by Nartex.
Made in Mexico by:
NARTEX
Laboratorios Homeopaticos,
S.A. de C.V.
Calz. Lazaro Cardenas 708-770 Ote.
Col. Eduardo Guerra
Torreon, Coah. Mexico C.P. 27280
www.nartexlabs.com
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
ARNICA MONTANA NARTEX
arnica montana, hamamelis virginiana creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:34666-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 1.73 g in 29.7 g HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) (HAMAMELIS VIRGINIANA LEAF - UNII:T07U1161SV) HAMAMELIS VIRGINIANA LEAF 0.0178 g in 29.7 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) LANOLIN (UNII: 7EV65EAW6H) GLYCERIN (UNII: PDC6A3C0OX) PARAFFIN (UNII: I9O0E3H2ZE) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:34666-001-10 1 in 1 CARTON 06/01/2007 1 29.7 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 homeopathic 06/01/2007 Labeler - NARTEX LABORATORIOS HOMEOPATICOS SA DE CV (589914576) Establishment Name Address ID/FEI Business Operations LABORATORIOS HOMEOPATICOS SA DE CV 589914576 manufacture(34666-001)