NDC 49726-005

Candidol Candida Overgrowth Sympton Relief

Abies Nigra, Antimonium Crudum, Asafoetida, Baptisia Tinctoria, Borax, Candida Albicans, Lachesis Mutus, Phosphoricum Acidum, Phytolacca Decandra, Pulsatilla, Sticta Pulmonaria, Sulphur, Thuja Occidentalis

Candidol Candida Overgrowth Sympton Relief is a Oral; Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Picea Mariana Resin; Antimony Trisulfide; Asafetida; Baptisia Tinctoria; Sodium Borate; Candida Albicans; Lachesis Muta Venom; Phosphoric Acid; Phytolacca Americana Root; Pulsatilla Vulgaris; Lobaria Pulmonaria; Sulfur; Thuja Occidentalis Leafy Twig.

Product ID49726-005_7df08284-237d-0914-e053-2991aa0aa0fa
NDC49726-005
Product TypeHuman Otc Drug
Proprietary NameCandidol Candida Overgrowth Sympton Relief
Generic NameAbies Nigra, Antimonium Crudum, Asafoetida, Baptisia Tinctoria, Borax, Candida Albicans, Lachesis Mutus, Phosphoricum Acidum, Phytolacca Decandra, Pulsatilla, Sticta Pulmonaria, Sulphur, Thuja Occidentalis
Dosage FormLiquid
Route of AdministrationORAL; TOPICAL
Marketing Start Date2010-01-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHello Life, Inc.
Substance NamePICEA MARIANA RESIN; ANTIMONY TRISULFIDE; ASAFETIDA; BAPTISIA TINCTORIA; SODIUM BORATE; CANDIDA ALBICANS; LACHESIS MUTA VENOM; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; LOBARIA PULMONARIA; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient Strength12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49726-005-02

1 BOTTLE in 1 CARTON (49726-005-02) > 59 mL in 1 BOTTLE
Marketing Start Date2010-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49726-005-02 [49726000502]

Candidol Candida Overgrowth Sympton Relief LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-07
Inactivation Date2020-01-31

Drug Details


Trademark Results [Candidol]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CANDIDOL
CANDIDOL
77002688 3221208 Live/Registered
DUOIBES, ALBERT
2006-09-19

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