FDA.reportPublic FDA data

Thymuline

Manufacturer
Ratis, LLC | Apotheca Company
Effective date
2022-03-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:06:47

Label at a glance#

ProductThymuline
Active ingredientNONATHYMULIN
Label structure9 sections

Dosage and administration

4-5 sprays under tongue or in a small glass of water once a week or as needed. Children 2-12: 2-3 sprays as above. For children 12 and under, consult a doctor. Store in a cool, dry place.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Thymuline 9C

INDICATIONS:

OTC - PURPOSE SECTION

Immune system support.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen or worsen, ask a health care professional.

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

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

4-5 sprays under tongue or in a small glass of water once a week or as needed. Children 2-12: 2-3 sprays as above. For children 12 and under, consult a doctor. Store in a cool, dry place.

INDICATIONS:

INDICATIONS & USAGE SECTION

Immune system support.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, Glycerin, Organic Ethanol 10%

QUESTIONS:

OTC - QUESTIONS SECTION

Questions? Comments?

Visit HomeopathyStore.com or call (888) 405-7551.

Distributed by: Ratis, LLC,

211 E Lombard St,

STE 303, Baltimore, MD 21202

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71753-1152-1

Anna's

REMEDIES

Thymuline

IMMUNE SYSTEM SUPPORT**

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

ThymulineThymuline

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-1152THYMULINE LIQUID [RATIS, LLC]2Legacy NDC20220309_8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca.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
71753-115271753-1152-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
NONATHYMULIN9H198D04WLACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT

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
ff94c869-5b3e-43a2-8935-9372fb2333fa8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca2022-03-08WarningsExact identifier
spl id: ff94c869-5b3e-43a2-8935-9372fb2333fa
spl set id: 8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca

Reported adverse events (FAERS/openFDA)#

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