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Shot Support

Manufacturer
Spectrum Awakening, LLC | HomeoCare Laboratories, Inc. | HomeoCare Laboratories Inc.
Effective date
2019-08-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:14:22

Label at a glance#

ProductShot Support
Active ingredientALUMINUM OXIDE, ALUMINUM, CALCIUM HYDROXIDE, SILICON DIOXIDE, ARNICA MONTANA, THUJA OCCIDENTALIS LEAF, SULFUR, MERCURIUS SOLUBILIS
Label structure8 sections

Indications and uses

For the self-limiting condition: Serum reaction due to vaccination or as directed by your doctor.

Dosage and administration

5 drops in the mouth or in water before bed or as directed by your doctor.

Label contents#

Full prescribing information#

Uses*:

INDICATIONS & USAGE SECTION

For the self-limiting condition: Serum reaction due to vaccination or as directed by your doctor.

Warnings:

WARNINGS SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen. Do not use if pregnant/breastfeeding. Keep out of reach of children

Directions:

DOSAGE & ADMINISTRATION SECTION

5 drops in the mouth or in water before bed or as directed by your doctor.

Uses*:

OTC - PURPOSE SECTION

For the self-limiting condition: Serum reaction due to vaccination or as directed by your doctor.

Other information:

OTHER SAFETY INFORMATION

Contains about 100 servings. Do not use if seal is broken.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Purified water, Ethanol 20%

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

12.5% each: Alumina 12X, Aluminum Metallicum 12X, Arnica 6X, Calcarea Caustica 12X, Mercurius solubilis 12X, Silicea 8X, Sulphur 8X, Thuja 30C.

Spectrum Awakening Shot Support*

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Homeopathic Drops

1 Fluid oz (30 ml)

For Professional Use Only

Distributed by: Spectrum Awakening

857 N Main St Ext Wallingford, CT 06492

www.SpectrumAwakening.com ShotSupportLabel.jpShotSupportLabel.jp

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73290-10073290-100-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM OXIDELMI26O6933ACTIB
ALUMINUMCPD4NFA903ACTIB
CALCIUM HYDROXIDEPF5DZW74VNACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
ARNICA MONTANAO80TY208ZWACTIB
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
SULFUR70FD1KFU70ACTIB
MERCURIUS SOLUBILIS324Y4038G2ACTIB
ALCOHOL3K9958V90MIACT
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
d3bf910e-e216-01e0-e053-2995a90a847690cf0ffe-de07-2625-e053-2a95a90a6bf52021-12-22WarningsExact identifier
spl set id: 90cf0ffe-de07-2625-e053-2a95a90a6bf5

Reported adverse events (FAERS/openFDA)#

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