Cannabis Sativa

Manufacturer
Remedy Makers
Effective date
2023-03-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:20:35

Label at a glance#

ProductCannabis Sativa
Active ingredientCANNABIS SATIVA FLOWERING TOP
Label structure11 sections

Dosage and administration

Take 1mL by mouth or as directed by a physician.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

CANNABIS SATIVA 1X

(Cannabidiol) 100mg per mL Delta 9 THC < 0.3%

OTC - PURPOSE SECTION

LESSENS PAIN, IMPROVES APPETITE, AND CAUSES SLEEP

WARNING:

WARNINGS SECTION

"The FDA has not determined that this product is safe, effective and not misbranded for its intended use."

INDICATIONS & USAGE SECTION

To be used according to standard homeopathic indications for self-limiting conditions such as those indicated above or as directed by a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children.

Warning:

WARNINGS SECTION

Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug, if you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.

Directions:

DOSAGE & ADMINISTRATION SECTION

Take 1mL by mouth or as directed by a physician.

Other information:

HOW SUPPLIED SECTION

Contains approx. 30 doses.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

MCT Oil, Alcohol, and Strawberry Flavoring. Free from yeast, wheat, corn, and soy.

Questions or comments

OTC - QUESTIONS SECTION

(877) REM4YOU Fax (909) 594-4205 Pomona, CA 91768. USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sample LabelSample Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10191-6374-12025-01-30C16284748780-12cef2736-69e9-d83d-e063-dadaa90ab31ff67ef4de-fd33-0fac-e053-2995a90af464

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-6374-1Cannabis Sativa30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-6374CANNABIS SATIVA LIQUID [REMEDY MAKERS]21 package rows20230323_f67ef4de-fd33-0fac-e053-2995a90af464.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10191-637410191-6374-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
f7844666-9d66-2c00-e053-6294a90aee29f67ef4de-fd33-0fac-e053-2995a90af4642023-03-22WarningsExact identifier
spl id: f7844666-9d66-2c00-e053-6294a90aee29
spl set id: f67ef4de-fd33-0fac-e053-2995a90af464

Reported adverse events (FAERS/openFDA)#

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