Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g)

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g)
Generic name: NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE)
Manufacturer: Reedfresh Co., LTD
Product type: HUMAN OTC DRUG
SPL set ID: 55d703ca-ff9d-0dbc-e063-6294a90ab6b1
SPL ID: 55d70467-cb7a-43d8-e063-6394a90a3446
Version: 1
Effective date: 2026-07-05
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:48

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g)	openfda.brand_name
generic name		NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE)	openfda.generic_name
manufacturer name		Reedfresh Co., LTD	openfda.manufacturer_name
ndc	package	85514-7538-1	openfda.package_ndc
ndc	product	85514-7538	openfda.product_ndc
ndc11	package	85514753801	derived:openfda.package_ndc
spl id		55d70467-cb7a-43d8-e063-6394a90a3446	id
spl set id		55d703ca-ff9d-0dbc-e063-6294a90ab6b1	set_id
unii		TR046Y3K1G	openfda.unii
unii		PDC6A3C0OX	openfda.unii
unii		059QF0KO0R	openfda.unii
unii		N8F53B3R4R	openfda.unii
unii		XJ7052W897	openfda.unii
unii		2DMT128M1S	openfda.unii
unii		C9H2L21V7U	openfda.unii
unii		3SCV180C9W	openfda.unii
unii		92RU3N3Y1O	openfda.unii
unii		230OU9XXE4	openfda.unii
unii		7GXZ3858RY	openfda.unii
unii		YD01N1999R	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Cautions: 1. Discontinue use if the following symptoms occur. Consult a dermatologist if symptoms persist. 1) Redness, swelling, itching, or irritation during use. 2) Similar symptoms appear on applied areas after sun exposure. 2. Do not use on wounds, eczema, or inflamed skin. 3. Avoid contact with eyes. Rinse immediately if contact occurs.

Reported adverse events (FAERS/openFDA)#

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