LuminousGlowBeautifyingLotion

Product NDC
84423-089
11-digit product format
844230089
Labeler code
84423
Product ID
84423-089_3b808fdc-fb0a-a34f-e063-6294a90ac947
Type
HUMAN OTC DRUG
Nonproprietary name
LuminousGlowBeautifyingLotion
Dosage form
EMULSION
Route
CUTANEOUS
Labeler
Guangzhou Kadiya Biotechnology Co., Ltd.
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-08-04
Substance
ARBUTIN; GLUTATHIONE; KOJIC ACID
Active strength
10; 4; 15 g/500g; g/500g; g/500g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
LuminousGlowBeautifyingLotion
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARBUTIN10 g/500g
GLUTATHIONE4 g/500g
KOJIC ACID15 g/500g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC5INA23HXF, GAN16C9B8O, 6K23F1TT52

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2dae634-14ed-febf-08ee-93196433b5b7Product name920190614
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
0a5e5249-329b-0cff-e714-77159f193a87Product name120140508
6b7a6f32-42a6-994d-5ab6-d180e92ee9d8Product name120140508
d394f843-7479-dc48-dbd3-232266c5548cProduct name120140508
dc9a5fb6-14e2-1cc8-a567-a781fd1f0212Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84423-089-01LuminousGlowBeautifyingLotion500 g in 1 BOTTLE, PLASTICEMULSION5001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84423-089-0184423008901500 g in 1 BOTTLE, PLASTIC (84423-089-01) 500 g2025-08-04NoNoHistorical