Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder) by

Drug Labeling and Warnings

Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder) by is a Otc medication manufactured, distributed, or labeled by HumanEnos LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BIO NO MORE YEAST INFECTION (HELPS IMPROVE VAGINAL YEAST INFECTION, FERMENTED CABBAGE POWDER)- nitric oxide, vitamin d3, glutathione tablet 
HumanEnos LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

900 mg / 0.032oz

KEEP OUT OF THE REACH OF CHILDREN.

Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

Warnings

Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

Inactive ingredients:

Glutathione, lettuce, Garlic

Active ingredients:

Nitric Oxide, Vitamin D3, Glutathione

37

BIO NO MORE YEAST INFECTION (HELPS IMPROVE VAGINAL YEAST INFECTION, FERMENTED CABBAGE POWDER) 
nitric oxide, vitamin d3, glutathione tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 83202-6447
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE100 mg  in 900 mg
Inactive Ingredients
Ingredient NameStrength
LETTUCE (UNII: 5PO6NN3RRJ) 1 mg  in 900 mg
GLUTATHIONE (UNII: GAN16C9B8O) 1 mg  in 900 mg
GARLIC (UNII: V1V998DC17) 1 mg  in 900 mg
Product Characteristics
ColorwhiteScorescore with uneven pieces
ShapeCAPSULESize900mm
FlavorFRUITImprint Code capsule
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 83202-6447-2900 mg in 1 PACKAGE; Type 0: Not a Combination Product01/01/202512/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/01/202512/31/2025
Labeler - HumanEnos LLC (695801540)
Establishment
NameAddressID/FEIBusiness Operations
HumanEnos LLC695801540manufacture(83202-6447)

Revised: 3/2025
 

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.