Label: CALENDULA OFFICINALIS spray
- NDC Code(s): 82969-6018-1
- Packager: Bestmade Natural Products
- 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 January 2, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- PURPOSE
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CALENDULA OFFICINALIS
calendula officinalis sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82969-6018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALENDULA OFFICINALIS WHOLE (UNII: PFR03EBU0H) (CALENDULA OFFICINALIS WHOLE - UNII:PFR03EBU0H) CALENDULA OFFICINALIS WHOLE 1 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 30 mL in 30 mL Product Characteristics Color white (transparent spray) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82969-6018-1 1 in 1 BOX 01/01/2020 1 30 mL in 1 BOTTLE; Type 6: Drug/Biologic Combination Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2020 Labeler - Bestmade Natural Products (047124582) Establishment Name Address ID/FEI Business Operations Total Operations Management LLC DBA: Bestmade Natural Products Micro 047124582 manufacture(82969-6018)

