NDC 57955-0815

Mole Remover

Carbo Vegetabilis, Graphites, Lycopodium Clavatum, Phytolacca Decandra, Thuja Occidentalis

Mole Remover is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Carbo Animalis; Graphite; Lycopodium Clavatum Spore; Phytolacca Americana Root; Thuja Occidentalis Leafy Twig.

Product ID57955-0815_f4f9ae92-8169-4e1b-8bf4-92da6e216dfa
NDC57955-0815
Product TypeHuman Otc Drug
Proprietary NameMole Remover
Generic NameCarbo Vegetabilis, Graphites, Lycopodium Clavatum, Phytolacca Decandra, Thuja Occidentalis
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2014-08-13
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameCARBO ANIMALIS; GRAPHITE; LYCOPODIUM CLAVATUM SPORE; PHYTOLACCA AMERICANA ROOT; THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient Strength10 [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 57955-0815-3

1 BOTTLE, WITH APPLICATOR in 1 CARTON (57955-0815-3) > 15 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Start Date2018-01-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-0815-3 [57955081503]

Mole Remover LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-12
Inactivation Date2020-01-31
Reactivation Date2020-05-13

Drug Details

Active Ingredients

IngredientStrength
CARBO ANIMALIS10 [hp_X]/15mL

OpenFDA Data

SPL SET ID:85f34a4a-1de4-4d49-8070-afce7fa803df
Manufacturer
UNII

NDC Crossover Matching brand name "Mole Remover" or generic name "Carbo Vegetabilis, Graphites, Lycopodium Clavatum, Phytolacca Decandra, Thuja Occidentalis"

NDCBrand NameGeneric Name
57955-0815Mole RemoverCarbo vegetabilis, Graphites, Lycopodium clavatum, Phytolacca decandra, Thuja occidentalis
68703-216Healthful Naturals Mole RemoverMole Remover

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.