- 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)