Blue Scorpion Pain and Inflammation Relief

Manufacturer
Blue Scorpion Inc.
Effective date
2024-01-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:25:43

Label at a glance#

ProductBlue Scorpion Pain and Inflammation Relief
Active ingredientAPIS MELLIFERA, TOXICODENDRON PUBESCENS LEAF, RHOPALURUS PRINCEPS VENOM
Label structure11 sections

Dosage and administration

Directions Adults and children 12 years and over: Administer 2 ml under tongue twice per day. Children under 12: Consult a physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Apis Mellifica 6X

Heteroctenus Princeps Venom 3X

Rhus Tox 6X

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years and over:Administer 2 ml under tongue twice per day.
Children under 12:Consult a physician.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Citric Acid, Distilled water

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 call a Poison Control Center right away.

INDICATIONS:

INDICATIONS & USAGE SECTION

Uses

  • For the temporary relief of pain and inflammation

PURPOSE:

OTC - PURPOSE SECTION

Hereroctenus princeps venom 3x.....Pain, inflammation
Apis Mellifica 6X ..............................Pain, inflammation
Rhus Tox 6X.....................................Pain, inflammation

If pregnant or breast feeding...

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTHER INFORMATION:

SPL UNCLASSIFIED SECTION

  • Refrigerate after opening
  • Do not freeze

Warning

WARNINGS SECTION

Stop use and ask doctor if symptoms persist for more than 3 days or worsen.

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal display panel

LabelLabel

Label 1 ozLabel 1 oz

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83627-901-01Blue Scorpion Pain and Inflammation Relief120 mL in 1 BOTTLELIQUID1203
83627-901-02Blue Scorpion Pain and Inflammation Relief30 mL in 1 BOTTLELIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83627-901BLUE SCORPION PAIN AND INFLAMMATION RELIEF (HETEROCTENUS PRINCEPS VENOM, APIS MELLIFICA, RHUS TOXICODENDRON) LIQUID [BLUE SCORPION INC.]3Current NDC, 2 package rows20240119_03ef74f2-46d3-345c-e063-6394a90a4cbf.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83627-90183627-901-01, 83627-901-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Blue Scorpion Pain and Inflammation ReliefHETEROCTENUS PRINCEPS VENOM, APIS MELLIFICA, RHUS TOXICODENDRONBlue Scorpion Inc.03ef74f2-46d3-345c-e063-6394a90a4cbf2024-01-16WarningsExact identifier
ndc (package): 83627-901-01
ndc (package): 83627-901-02
ndc (product): 83627-901
ndc11 (package): 83627090102
ndc11 (package): 83627090101
spl id: 0f1db862-53a5-9df7-e063-6394a90a241f
spl set id: 03ef74f2-46d3-345c-e063-6394a90a4cbf

Reported adverse events (FAERS/openFDA)#

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