Label: ARTHRONEW PM- not applicable gel
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Contains inactivated NDC Code(s)
NDC Code(s): 61045-0002-1 - Packager: PureCore Wellness, Inc
- 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 November 6, 2014
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
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INACTIVE INGREDIENTS:
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALOE BARBADENSIS LEAF JUICE, ARNICA (FLOWER), ASCORBIC ACID, DEVIL'S CLAW (ROOT), EDETATE DISODIUM (EDTA), MIXED TOCOPHEROLS [VITAMIN E] (DERIVED FROM SOY BEAN), NATURAL PLANT EXTRACT, PEG-33, PEG-8 DIMETHICONE, PEG-14, PEPPERMINT (LEAF), PHENOXYETHANOL, CAPRYLYL GLYCOL, SORBIC ACID, POTASSIUM SORBATE, PURIFIED WATER, SODIUM HYDROXIDE, WHITE WILLOW (BARK), WITCH HAZEL (BARK)
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ARTHRONEW PM
not applicable gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61045-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X] in 1 g HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X] in 1 g TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 6 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) ALOE VERA LEAF (UNII: ZY81Z83H0X) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASCORBIC ACID (UNII: PQ6CK8PD0R) HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89) EDETATE DISODIUM (UNII: 7FLD91C86K) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) OREGANO (UNII: 0E5AT8T16U) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) PEG-8 DIMETHICONE (UNII: GIA7T764OD) POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R) MENTHA PIPERITA LEAF (UNII: A389O33LX6) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SORBIC ACID (UNII: X045WJ989B) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SALIX ALBA BARK (UNII: 205MXS71H7) HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61045-0002-1 57 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/03/2014 Labeler - PureCore Wellness, Inc (079158894) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(61045-0002) , api manufacture(61045-0002) , label(61045-0002) , pack(61045-0002)