Scarstat

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:28:38

Label at a glance#

ProductScarstat
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, GRAPHITE, HYPERICUM PERFORATUM WHOLE, SILICON DIOXIDE, DELPHINIUM STAPHISAGRIA SEED, ALLYLTHIOUREA
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 9.08% Calendula Officinalis 10X, 6C, Graphites 10X, 6C, Hypericum Perforatum 10X, 6C, Silicea 10X, Staphysagria 10X, 6C, Thiosinaminum 10X, 6C; 0.10% of Silicea 6C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve discomfort from scar tissue due to old scars and keloids.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

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

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of old scar tissue discomfort; scar tissue; old scars; and keloids.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

SCARSTAT

1 fl. oz. (30 ml)

SCARSTATSCARSTAT

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0149-12024-10-30C16284748780-1ba0f9c33-5a54-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0149-12024-01-30C16284748780-1ba0f9c33-5a54-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0149-12022-02-11C16284748780-1ba0f9c33-5a54-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0149-12021-01-29C16284748780-1ba0f9c33-5a54-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0149-1Scarstat30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0149SCARSTAT (CALENDULA OFFICINALIS, GRAPHITES, HYPERICUM PERFORATUM, SILICEA, STAPHYSAGRIA, THIOSINAMINUM) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241101_1decc2eb-1261-46b8-908e-a152535b4a02.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALLYLTHIOUREAACTIVE INGREDIENT706IDJ14B71
CALENDULA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT18E7415PXQ1
DELPHINIUM STAPHISAGRIA SEEDACTIVE INGREDIENT00543AP1JV1
GRAPHITEACTIVE INGREDIENT4QQN74LH4O1
HYPERICUM PERFORATUMACTIVE INGREDIENTXK4IUX8MNB1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
ALLYLTHIOUREAACTIVE MOIETY706IDJ14B71
CALENDULA OFFICINALIS FLOWERING TOPACTIVE MOIETY18E7415PXQ1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
DELPHINIUM STAPHISAGRIA SEEDACTIVE MOIETY00543AP1JV1
GRAPHITEACTIVE MOIETY4QQN74LH4O1
HYPERICUM PERFORATUMACTIVE MOIETYXK4IUX8MNB1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-014944911-0149-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
ScarstatCALENDULA OFFICINALIS, GRAPHITES, HYPERICUM PERFORATUM, SILICEA, STAPHYSAGRIA, THIOSINAMINUMEnergique, Inc.1decc2eb-1261-46b8-908e-a152535b4a022024-10-30WarningsExact identifier
ndc (package): 44911-0149-1
ndc (product): 44911-0149
ndc11 (package): 44911014901
spl id: 2292102b-c953-4a31-a627-62382d5ce12a
spl set id: 1decc2eb-1261-46b8-908e-a152535b4a02

Reported adverse events (FAERS/openFDA)#

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