Neuroquell-Plus

Manufacturer
Atlantic Management Resources Inc
Effective date
2022-07-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:17:43

Label at a glance#

ProductNeuroquell-Plus
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

WARNINGS SECTION

WarningsWarnings

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of ChildrenKeep out of reach of Children

OTC - PURPOSE SECTION

OTC Purpose sectionOTC Purpose section

DOSAGE & ADMINISTRATION SECTION

When you are ready to apply Neuroquell, remove the cap, turn the bottle upside down, and gently roll the applicator onto the area of discomfort in a continuous, back-and-forth motion to cover approximately one-half of the area of your pain. If using either the sample swab or towelette, apply in a similar way. Your skin will remain moist for a few minutes. Close cap tightly after use, and wash hands thoroughly. Feel free to reapply 4-to-6 hours later and up to 3 additional times per day. To eliminate the peppermint scent, you can wash the treated area with soap and water 15 minutes after the application. This will not affect the efficacy of the product. If there is highlights text then the SPL document title should include the following text string without quotation marks: These highlights do not include all the information needed to use see full prescribing information for and Initial U.S. Approval

INDICATIONS & USAGE SECTION

Temporarily relieves pain associated with minor aches and pains of muscles, joints, nerve-based pain and headaches/migraines. Individual results may vary.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neuroquell-Plus LabelNeuroquell-Plus Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66233-714-012024-01-30C16284748780-1d6a99b39-3876-a426-e053-dadaa90af4c2Neuroquell-Plus
66233-714-012022-07-11C16284748780-1d6a99b39-3876-a426-e053-dadaa90af4c2Neuroquell-Plus
66233-714-012022-01-28C16284748780-1d6a99b39-3876-a426-e053-dadaa90af4c2Neuroquell-Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66233-714-01Neuroquell-Plus1 g in 1 BOTTLE, WITH APPLICATOROIL14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66233-714NEUROQUELL-PLUS OIL [ATLANTIC MANAGEMENT RESOURCES INC]4Legacy NDC, 1 package rows20220713_2835db18-ff79-542e-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66233-71466233-714-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
e38c7016-9cf5-0599-e053-2a95a90a2b1b2835db18-ff79-542e-e054-00144ff8d46c2022-07-11WarningsExact identifier
spl id: e38c7016-9cf5-0599-e053-2a95a90a2b1b
spl set id: 2835db18-ff79-542e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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