FDA.reportPublic FDA data

Derma Rash HP

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:48

Label at a glance#

ProductDerma Rash HP
Active ingredientARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, GRAPHITE, MERCURIUS SOLUBILIS, DAPHNE MEZEREUM BARK, KEROSENE, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, SULFUR
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times 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): 11.11% of Arsenicum Album 30X, Calcarea Carbonica 30X, Graphites 30X, Mercurius Solubilis 30X, Mezereum 30X, Petroleum 30X, Rhus Tox 30X, Sepia 30X, Sulphur 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms due to skin irritation and chronic skin eruptions.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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

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 times 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

May temporarily relieve symptoms due to skin irritation and chronic skin eruptions.**

**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
DERMA RASH HP
1 fl. oz. (30 ml)

DERMA RASH HPDERMA RASH HP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0567-12024-01-23C16284748780-1f386c64a-423f-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0567-12023-01-30C16284748780-1f386c64a-423f-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0567-1Derma Rash HP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0567DERMA RASH HP (ARSENICUM ALBUM, CALCAREA CARBONICA, GRAPHITES, MERCURIUS SOLUBILIS, MEZEREUM, PETROLEUM, RHUS TOX, SEPIA, SULPHUR) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20240124_7d3b8655-f1f3-4389-8c0d-7e4fb0b00434.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-056744911-0567-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIOXIDES7V92P67HOACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
GRAPHITE4QQN74LH4OACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
DAPHNE MEZEREUM BARKX2N6E405GVACTIB
KEROSENE1C89KKC04EACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Derma Rash HPARSENICUM ALBUM, CALCAREA CARBONICA, GRAPHITES, MERCURIUS SOLUBILIS, MEZEREUM, PETROLEUM, RHUS TOX, SEPIA, SULPHUREnergique, Inc.7d3b8655-f1f3-4389-8c0d-7e4fb0b004342024-01-23WarningsExact identifier
ndc (package): 44911-0567-1
ndc (product): 44911-0567
ndc11 (package): 44911056701
spl id: 6586c197-e037-41b3-9feb-c3026ddc66f2
spl set id: 7d3b8655-f1f3-4389-8c0d-7e4fb0b00434

Reported adverse events (FAERS/openFDA)#

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