Deep Repair DARK SPOT

Manufacturer
Deep Repair DARK SPOT
Effective date
2024-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:33:22

Label at a glance#

ProductDeep Repair DARK SPOT
Active ingredientINOSITOL, 3-O-ETHYL ASCORBIC ACID, ALPHA-ARBUTIN, NIACINAMIDE, CENTELLA ASIATICA
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Active ingredient (in each 50ml) Purpose
Niacinamide 1500mg.
Inositol 1000mg.
Alpha-Arbutin 125 mg.
3-0-Ethyl Ascorbic Acid 100 mg
Centella Asiatica Extract 99.2mg

OTC - PURPOSE SECTION


Deep Repair DARKSPOT
Corrector

INACTIVE INGREDIENT SECTION


Aqua,Glycerin,Propylene
Glycol,Caprylic/Capric Triglyceride,Cetearyl
Alcohol,Dimethicone,Butyrospermum Parkii
(Shea) Butter, Glyceryl Stearate,Hexanediol,
Hydroxyacetophenone,Squalane,Tocopheryl
Arginine,Carbomeracetate,Peg-100 Stearate,
Cetearyl,Glucoside,Phenoxyethanol,Arginine,
Carbomer,Pelargonium Graveolens Extract,
Polysorbate 80,Ethylhexylglycerin,Sodium
Hyaluronate,Mentha Arvensis Leaf Extract,Aloe
Barbadensis Extract,Sorbitan Oleate,Sophora
Angustifolia Root Extract,Fragrance,Disodium
Edta

WARNINGS SECTION


If pregnant or breast-feading, ask a health
professional before use. Keep out of reach of
children. In case of overdose,got medical help
or contact a Poison Control Center right away.

OTC - STOP USE SECTION


If pregnant or breast-feading, ask a health
professional before use. Keep out of reach of
children. In case of overdose,got medical help
or contact a Poison Control Center right away.

OTC - DO NOT USE SECTION


If pregnant or breast-feading, ask a health
professional before use. Keep out of reach of
children. In case of overdose,got medical help
or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of children. In case of overdose,got medical help
or contact a Poison Control Center right away.

OTC - WHEN USING SECTION


When using this productSwipe onto a clean face, morning and/or evening
mDo not rinse.
For daytime use, follow with sunscreen

INDICATIONS & USAGE SECTION


Uses
Uneven skin tone
Spot removal for desired area

DOSAGE & ADMINISTRATION SECTION

take appropriate cream to the dark area

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelingpackage labeling

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84867-001-012026-01-29C16284748780-149896155-aa78-586f-e063-e6dba90add9025eb7919-0fbf-34de-e063-6294a90a7481

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84867-001-01Deep Repair DARK SPOT50 mL in 1 BOTTLE, PLASTICCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84867-001DEEP REPAIR DARK SPOT CREAM [DEEP REPAIR DARK SPOT]11 package rows20241103_25eb7919-0fbf-34de-e063-6294a90a7481.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
84867-00184867-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
25eb7919-0fc0-34de-e063-6294a90a748125eb7919-0fbf-34de-e063-6294a90a74812024-11-02WarningsExact identifier
spl id: 25eb7919-0fc0-34de-e063-6294a90a7481
spl set id: 25eb7919-0fbf-34de-e063-6294a90a7481

Reported adverse events (FAERS/openFDA)#

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