NDC 0360-0004

ACONITE

Aconite Napellus

ACONITE is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Standard Homeopathic Company. The primary component is Aconitum Napellus.

Product ID0360-0004_7d9f1d26-1b02-0a20-e053-2991aa0a25df
NDC0360-0004
Product TypeHuman Otc Drug
Proprietary NameACONITE
Generic NameAconite Napellus
Dosage FormTablet
Route of AdministrationSUBLINGUAL
Marketing Start Date1997-02-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSTANDARD HOMEOPATHIC COMPANY
Substance NameACONITUM NAPELLUS
Active Ingredient Strength30 [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0360-0004-02

1 g in 1 BOTTLE, PLASTIC (0360-0004-02)
Marketing Start Date1997-02-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0360-0004-02 [00360000402]

ACONITE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1997-02-17

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS30 [hp_X]/g

OpenFDA Data

SPL SET ID:2e460cbe-17f9-4adf-e054-00144ff88e88
Manufacturer
UNII
UPC Code
  • 0300360000420
  • NDC Crossover Matching brand name "ACONITE" or generic name "Aconite Napellus"

    NDCBrand NameGeneric Name
    0360-0004ACONITEACONITE NAPELLUS
    44911-0152AconiteAconitum Napellus
    44911-0209ACONITEAconitum napellus
    57556-010Aconitum napellusAconite
    62106-7197ACONITUM NAPELLUSAconite

    Trademark Results [ACONITE]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACONITE
    ACONITE
    97890144 not registered Live/Pending
    Shenzhen Kelanqi Trading Co., Ltd.
    2023-04-15

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.