Label: CAPSIVA- capsicum annuum, arnica montana gel
- NDC Code(s): 72522-103-03, 72522-103-25, 72522-103-33
- Packager: ANESIS LIFE, LLC
- 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 October 27, 2023
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
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Warnings
For external use only
When using this product
- use only as directed
- avoid contact with eyes and open wounds
- in case of accidental contact with eyes, immediately flush with water and seek professional help
- do not apply local heat (such as heating pads) to the area of use
- do not cover or bandage
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CAPSIVA
capsicum annuum, arnica montana gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72522-103 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 84 g CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM 1 [hp_X] in 84 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) SALICYLIC ACID (UNII: O414PZ4LPZ) CUCUMBER (UNII: YY7C30VXJT) BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) SORBIC ACID (UNII: X045WJ989B) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72522-103-03 1 in 1 CARTON 05/06/2022 1 84 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:72522-103-25 1 in 1 CARTON 05/06/2022 2 35 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:72522-103-33 9.36 g in 1 POUCH; Type 0: Not a Combination Product 05/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/06/2022 Labeler - ANESIS LIFE, LLC (081342274) Establishment Name Address ID/FEI Business Operations BIOLYTE LABORATORIES, LLC 015560564 manufacture(72522-103)