Thymuline by Ratis, LLC / Apotheca Company THYMULINE liquid

Thymuline by

Drug Labeling and Warnings

Thymuline by is a Homeopathic medication manufactured, distributed, or labeled by Ratis, LLC, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Thymuline 9C

INDICATIONS:

Immune system support.**

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

WARNINGS:

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:

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

DIRECTIONS:

5 sprays under tongue once a week or as needed. For children 12 and under, consult a doctor. Store in a cool, dry place.

INDICATIONS:

Immune system support.**

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

INACTIVE INGREDIENTS:

Demineralized Water, Glycerin, Organic Ethanol 10%

QUESTIONS:

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:

NDC: 71753-1052-1

Anna's

REMEDIES

Thymuline

IMMUNE SYSTEM SUPPORT**

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

INGREDIENTS AND APPEARANCE

THYMULINE 
thymuline liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71753-1052
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NONATHYMULIN (UNII: 9H198D04WL) (NONATHYMULIN - UNII:9H198D04WL)	NONATHYMULIN	9 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71753-1052-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/03/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/03/2017

Labeler - Ratis, LLC (964594324)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(71753-1052) , api manufacture(71753-1052) , label(71753-1052) , pack(71753-1052)