Bio NO more Joint Pain (Helps improve osteoarthritis and Immunity, Soybean and oplopanax elatus Nakai fermented powder)

Bio NO more Joint Pain (Helps improve osteoarthritis and Immunity, Soybean and oplopanax elatus Nakai fermented powder) by

Drug Labeling and Warnings

Bio NO more Joint Pain (Helps improve osteoarthritis and Immunity, Soybean and oplopanax elatus Nakai fermented 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 JOINT PAIN (HELPS IMPROVE OSTEOARTHRITIS AND IMMUNITY, SOYBEAN AND OPLOPANAX ELATUS NAKAI FERMENTED POWDER)- nitric oxide, zinc, n-acetylglucosamine capsule 
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.

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Bio NO more Joint Pain (Helps improve osteoarthritis and Immunity, Soybean and oplopanax elatus Nakai fermented powder)

800 mg X 120
/3.39 oz

KEEP OUT OF THE REACH OF CHILDREN.

Bio N:O more Joint Pain

Warnings

Bio N:O more Joint Pain

Inactive ingredients:

Oplopanax elatus nakai extract powder, yeast extract, crystalline cellulose

Active ingredients:

Nitric Oxide, Zinc, N-Acetylglucosamine

BIO NO MORE JOINT PAIN (HELPS IMPROVE OSTEOARTHRITIS AND IMMUNITY, SOYBEAN AND OPLOPANAX ELATUS NAKAI FERMENTED POWDER) 
nitric oxide, zinc, n-acetylglucosamine capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83202-6921
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH)	NITRIC OXIDE	100 mg  in 800 mg

Inactive Ingredients
Ingredient Name	Strength
OPLOPANAX ELATUS WHOLE (UNII: R7PZA0P44T)	1 mg  in 800 mg
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)	1 mg  in 800 mg

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	CAPSULE	Size	800mm
Flavor	FRUIT	Imprint Code	capsule
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83202-6921-1	120 mg in 1 PACKAGE; Type 0: Not a Combination Product	02/14/2023	03/04/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/14/2023	03/04/2023

Labeler - HumanEnos LLC (695801540)

Establishment
Name	Address	ID/FEI	Business Operations
HumanEnos LLC		695801540	manufacture(83202-6921)

Revised: 3/2023

Document Id: f61a0c5f-f537-580c-e053-2995a90ae88a

34390-5

Set id: f501598c-9fcc-a203-e053-2a95a90a6148

Version: 2

Effective Time: 20230304