FDA.reportPublic FDA data

Bliss Republic Dark Spot Wand

Manufacturer
Sargass Group Limited Liability Company
Effective date
2024-02-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:08:43

Label at a glance#

ProductBliss Republic Dark Spot Wand
Active ingredientNIACINAMIDE
Label structure12 sections

Dosage and administration

Age: 18+ Use once a day (morning or evening) to well-cleansed skin Apply sparingly and directly to dark spots.

Storage and handling

Always wear daily sunscreen of SPF 15 or higher when used on very dark skin. The lighting effect of this product may not be noticeable. Limit sun exposure to prevent reoccurrence of darkening.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 2%................. Reduce Dark Spots

Purpose

OTC - PURPOSE SECTION

Reduce Dark Spots

Use

INDICATIONS & USAGE SECTION

To reduce Dark Spots on the skin

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

Avoid contact with eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children. Avoid contact with eyes. In case of accidental ingestion, seek medical attention immefiately.

OTC - STOP USE SECTION

Discontinue use if no improvement is seen after 3 months of treatment.

Directions

DOSAGE & ADMINISTRATION SECTION

Age: 18+ Use once a day (morning or

evening) to well-cleansed skin

Apply sparingly and directly

to dark spots.

Other information

STORAGE AND HANDLING SECTION

Always wear daily sunscreen of SPF 15 or higher when used on very dark skin.

The lighting effect of this product may not be noticeable.

Limit sun exposure to prevent reoccurrence of darkening.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Isobutane, Erythritol, Angelica keiskei extract, Hydrolyzed

collagen, Phloretin, Stephania tetrandra extract, Paeonia veitchii root extract, Propane, Carbomer, Dimethyl ether, Taraxacum officinale

(dandelion) leaf extract, 3-0-Ethyl ascorbic acid, Saururus chinensis extract,

Hyaluronic acid, Phenoxyethanol, Ethylhexylglycerin, Tranexamic acid,

Turmeric root extract, Kojic acid, Salicylic acid, Floral Scent.

RECENT MAJOR CHANGES SECTION

BLISS REPUBLIC DARK SPOT WAND

Turmeric, Niacinamide, Tranexamic Acid, Kojic Acid

Erase DarkSpots
Promote Uniformity
Reveal Radiant Skin Clarity

Customer Care:

For any questions, please contact us for a quick and satisfactory solution:

info@sargassgroup.com

Distributed by Sargass Group LLC, Casper, WY 82601

312 W 2nd St, A3007

+1 307 333 9039

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Darkspot-15Darkspot-1530mL NDC: 84028-112-11

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8234c772-5c41-424c-a33e-e06e8c4de9c1Product name220250626
fbe2ea47-480e-f5f1-0d64-c87fd5ac923bProduct name420250224
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
510b43a3-8143-a25f-19c6-476c90dbb618Product name920171115

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84028-112-112026-01-29C16284748780-149896155-de8d-586f-e063-e6dba90add90BLISS REPUBLIC Dark Spot Wand
84028-112-122026-01-29C16284748780-149896155-de8d-586f-e063-e6dba90add90BLISS REPUBLIC Dark Spot Wand

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84028-112-11Bliss Republic Dark Spot Wand15 mL in 1 BOTTLESOLUTION153
84028-112-12Bliss Republic Dark Spot Wand30 mL in 1 BOTTLESOLUTION303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84028-112BLISS REPUBLIC DARK SPOT WAND (DARK SPOT WAND) SOLUTION [SARGASS GROUP LIMITED LIABILITY COMPANY]32 package rows20240217_0f491a4d-6e0c-605b-e063-6394a90adb9c.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84028-11284028-112-11, 84028-112-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPANET75W9911L6IACT
TURMERIC856YO1Z64FIACT
NIACINAMIDE25X51I8RD4ACTIB
3-O-ETHYL ASCORBIC ACID6MW60CB71PIACT
PAEONIA VEITCHII ROOTVX6GD6M93VIACT
PHLORETINS5J5OE47MKIACT
STEPHANIA TETRANDRA ROOT48PS81XHK0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
TRANEXAMIC ACID6T84R30KC1IACT
GLYCERINPDC6A3C0OXIACT
ISOBUTANEBXR49TP611IACT
ANGELICA KEISKEI ROOT4LA4RT8O6PIACT
SAURURUS CHINENSIS FLOWER9L0SCP0SKZIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
KOJIC ACID6K23F1TT52IACT
DIMETHYL ETHERAM13FS69BXIACT
TARAXACUM OFFICINALE LEAF0022LFJ74YIACT
SALICYLIC ACIDO414PZ4LPZIACT
HYALURONIC ACIDS270N0TRQYIACT
HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)2WID9OCG7PIACT
ERYTHRITOLRA96B954X6IACT
WATER059QF0KO0RIACT

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
118070b1-4b71-a8ab-e063-6394a90a86960f491a4d-6e0c-605b-e063-6394a90adb9c2024-02-16WarningsExact identifier
spl id: 118070b1-4b71-a8ab-e063-6394a90a8696
spl set id: 0f491a4d-6e0c-605b-e063-6394a90adb9c

Reported adverse events (FAERS/openFDA)#

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