Label: 365 EVERYDAY VALUE ARNICA- arnica montana gel
- NDC Code(s): 42681-0512-5, 42681-0512-6
- Packager: WFM Private Label, LP
- 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 July 18, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- QUESTIONS
- PREGNANCY OR BREAST FEEDING
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
365 EVERYDAY VALUE ARNICA
arnica montana gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42681-0512 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 [hp_X] Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42681-0512-5 1 in 1 BOX; Type 0: Not a Combination Product 09/01/2008 2 NDC:42681-0512-6 1 in 1 BOX; Type 0: Not a Combination Product 01/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2008 Labeler - WFM Private Label, LP (196175616)