NO more Drip Nasal Spray (Relieves nasal congestion and sinus congestion, rehydrate nasal passages, allergy relief, Concentrated Lettuce fermentation solubles)

NO more Drip (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation) by

Drug Labeling and Warnings

NO more Drip (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation) by is a Otc medication manufactured, distributed, or labeled by HumanEnos LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NO MORE DRIP (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION)- ntric oxide liquid 
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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NO more Drip Nasal Spray (Relieves nasal congestion and sinus congestion, rehydrate nasal passages, allergy relief, Concentrated Lettuce fermentation solubles)

20 ml/ 0.7 oz

KEEP OUT OF THE REACH OF CHILDREN

N:O more Drip Nasal Spray

Warnings

N:O more Drip Nasal Spray

Inactive ingredients:

Lettuce

Active ingredients:

Ntric Oxide

NO MORE DRIP (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION) 
ntric oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83202-1468
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH)	NITRIC OXIDE	10 mg  in 20 mg

Inactive Ingredients
Ingredient Name	Strength
LETTUCE (UNII: 5PO6NN3RRJ)	1 mg  in 20 mg

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	CAPSULE	Size	20mm
Flavor	FRUIT	Imprint Code	capsule
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83202-1468-3	20 mg in 1 CAPSULE; 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(83202-1468)

Revised: 3/2023

Document Id: f6196a8c-84ac-20c2-e053-2995a90a41ea

34390-5

Set id: f501cbed-3109-efbf-e053-2a95a90a18e7

Version: 2

Effective Time: 20230304