AJOLOTIUS

Manufacturer
Camacho Navarrete, Jose Luis
Effective date
2024-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:58

Label at a glance#

ProductAJOLOTIUS
Active ingredientEUCALYPTUS GLOBULUS LEAF
Label structure11 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Do not give this product for persistent or chronic cough such as occurs with asthma or if cough is accompanied by excesive phlegm (mucus) unles directed by a doctor.
Stop use and ask a doctor if cough persist for more than 1 week, tends to recur or is accompanied by fever, rash or persistent headache, as a persistent cough may be a sing of a serious condition.
If pregnant or breast feeding, ask a health professional before use.

INDICATIONS & USAGE SECTION

For the relief of the symptoms of the common cold and cough.

DOSAGE & ADMINISTRATION SECTION

Children over 2 years take one teaspoon (2.5 mL) every 6 hours during the day.
Adults: Take one jtablespoon (5 mL) every 6 hours during the day.

DOSAGE FORMS & STRENGTHS SECTION

Oral administration.

CONTRAINDICATIONS SECTION

Hypersensitivity to the components of the formula.
Do not administer to children under 2 years of age, or to diabetic patients without medical supervision.

Do not use during pregnancy and breastfeeding without medical supervision.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medial help or contact a Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - ACTIVE INGREDIENT SECTION

EUCALYPTUS GLOBULUS LEAF

INACTIVE INGREDIENT SECTION

VERBASCUM THAPSUS
INVERT SUGAR
MENTHA PIPERITA
WATER
BOUGAINVILLEA GLABRA FLOWER

OTC - PURPOSE SECTION

For the relief of the symptoms of the common cold and cough.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84370-102-01 250 mL Label250 mL Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84370-102-012025-07-29C16284748780-13b156c62-2b01-fb37-e063-e6dba90a4e071cdae0f0-ea0d-9f72-e063-6394a90a7609

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84370-102-01AJOLOTIUS250 g in 1 BOTTLESYRUP2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84370-102AJOLOTIUS (SYRUP PLANT MIX) SYRUP [CAMACHO NAVARRETE, JOSE LUIS]11 package rows20240711_1cdae0f0-ea0d-9f72-e063-6394a90a7609.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84370-10284370-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
1cdae0f0-ea0e-9f72-e063-6394a90a76091cdae0f0-ea0d-9f72-e063-6394a90a76092024-01-06WarningsExact identifier
spl id: 1cdae0f0-ea0e-9f72-e063-6394a90a7609
spl set id: 1cdae0f0-ea0d-9f72-e063-6394a90a7609

Reported adverse events (FAERS/openFDA)#

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