Label: ARNICA GEL- arnica gel
- NDC Code(s): 0363-0139-26
- Packager: WALGREENS
- Category: HUMAN OTC DRUG LABEL
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 15, 2021
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- Drug facts
- Active ingredient
- Inactive ingredients
- Dosage and administration
- Uses*
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Warnings
For external use only. Avoid contact with eyes, mucous membranes, damaged skin, or wounds.
Do not use if you are allergic to Arnica montana or to any of thus product's inactive ingredients.
When using this product
- use only as directed
- do not bandage tightly or use a heating pad.
Stop use and ask a doctor if condition persists for more than 3 days or worsens.
- keep out of reach of children
- PURPOSE
- Other information
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARNICA GEL
arnica gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0139 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] in 1 g Inactive Ingredients Ingredient Name Strength CARBOMER 940 (UNII: 4Q93RCW27E) SODIUM HYDROXIDE (UNII: 55X04QC32I) ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0139-26 74 g in 1 PACKAGE; Type 0: Not a Combination Product 07/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/15/2021 Labeler - WALGREENS (008965063)