Nitric Oxide

Manufacturer
HumanEnos LLC
Effective date
2023-02-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:36:20

Label at a glance#

ProductDr. GNO Premium Soothing Gel (Brightening, Wrinckle care, and Moisturizing effect, Acne treatment, Fermented Lettuce ...
Active ingredientNITRIC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dr.GN:O Premium Soothing Gel

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.

INDICATIONS & USAGE SECTION

Dr.GN:O Premium Soothing Gel

WARNINGS SECTION

Warnings

OTC - PURPOSE SECTION

Dr.GN:O Premium Soothing Gel

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Aloe Barbadensis Leaf Extract, Houttuynia cordata extract

OTC - ACTIVE INGREDIENT SECTION

Active ingredients:

Nitric Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2121

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83202-665883202-6658-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
NITRIC OXIDE31C4KY9ESHACTIB
HOUTTUYNIA CORDATA WHOLEO3E12ZLW5TIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f516e416-4468-8f21-e053-2a95a90afd88f516e416-4467-8f21-e053-2a95a90afd882023-02-18WarningsExact identifier
spl id: f516e416-4468-8f21-e053-2a95a90afd88
spl set id: f516e416-4467-8f21-e053-2a95a90afd88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.