FDA.reportPublic FDA data

Converthera NAD plus Patch

Manufacturer
Through Medical INC.
Effective date
2025-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:49

Label at a glance#

ProductConverthera NAD plus Patch
Active ingredientNICOTINAMIDE ADENINE DINUCLEOTIDE, GLUTATHIONE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Apply the patch to skin firmly.
Leave on for 4-6 hours, then remove and discard.
Use 1-2 patches per week as needed or as directed by a licensed provider.

WARNINGS SECTION

Warnings:
For external use only. Do not exceed the recom- mended dose. Do not apply to broken, irritated, or sensitive skin. Mild redness or tingling may occur and is considered normal. Discontinue use if irritation or rash develops. Pregnant or nursing mothers, children under 18, or individu- als with known medical conditions should consult a physician before use. KEEP OUT OF REACH OF CHILDREN. DO NOT USE IF SAFETY SEAL IS DAMAGED OR MISSING. STORE IN A COOL, DRY PLACE.

INACTIVE INGREDIENT SECTION

Other Ingredients: Transdermal patch layer with hydrogel matrix and backing film.

INDICATIONS & USAGE SECTION

Clean a dry, hair-free area (upper arm, abdomen, or back).
Add 8-10 drops of NAD+ solution to the patch.
Apply the patch to skin firmly.
Leave on for 4-6 hours, then remove and discard.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - ACTIVE INGREDIENT SECTION

NAD+
(Nicotinamide Adenine
250 mg

Dinucleotide)
Vitamin B12
15,000 mcg

Glutathione

OTC - PURPOSE SECTION

Use 1-2 patches per week as needed or as directed by a licensed provider.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Content of LabelingContent of LabelingLabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85945-0001-1Converthera NAD plus Patch30 U in 1 PATCHPATCH301
85945-0001-2Converthera NAD plus Patch8 U in 1 PATCHPATCH81

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85945-000185945-0001-1, 85945-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
NICOTINAMIDE ADENINE DINUCLEOTIDE0U46U6E8UKACTIB
GLUTATHIONEGAN16C9B8OACTIB
LACTOSEJ2B2A4N98GIACT
GLUTENINFX065C7O71IACT

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
3a33f86a-c86c-9023-e063-6394a90a0f393a33f86a-c86b-9023-e063-6394a90a0f392025-07-18WarningsExact identifier
spl id: 3a33f86a-c86c-9023-e063-6394a90a0f39
spl set id: 3a33f86a-c86b-9023-e063-6394a90a0f39

Reported adverse events (FAERS/openFDA)#

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