Anatra

Manufacturer
Anatra LLC
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:38:07

Label at a glance#

ProductAnatra
Active ingredientCAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Label structure9 sections

Indications and uses

Temporarily relieves cold & flu-like symptoms such as: Body aches Headache Fever Chills Fatigue

Dosage and administration

ANATRA may be taken regularly as a preventative. Adults and children 2 years of age and older: Dissolve entire tablet in mouth every 6 hours, up to 3 times a day. Children under two years of age: Ask a Doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Anas barbariae. HPUS - 200 CK

Purpose

OTC - PURPOSE SECTION

To reduce the duration and severity of cold & flu-like symptoms. The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopeia of the United States.

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves cold & flu-like symptoms such as:

  • Body aches
  • Headache
  • Fever
  • Chills
  • Fatigue

Warnings

WARNINGS SECTION

Ask a Doctor before usein children under 2 years of age.
Stop use and ask a Doctor if symptoms persist for more than 3 days or worsen.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

ANATRA may be taken regularly as a preventative.
Adults and children 2 years of age and older: Dissolve entire tablet in mouth every
6 hours, up to 3 times a day. Children under two years of age: Ask a Doctor.

Other Information

SPL UNCLASSIFIED SECTION

Do not use if carton is open and/or bottle is open.Each 0.775g dose contains 0.5g of sugar. Store at 68-77°F (20-25°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beta Carotene, Citric Acid, Crospovidone, Dextrose,Lactose, Magnesium Stearate, Nat. Orange Flavor, Reb. A (Stevia LeafExtract), Silicon Dioxide, Stearic Acid

Questions/Comments?

SPL UNCLASSIFIED SECTION

Distributed by Anatra LLC 3250 NE 1st Ave., Suite 305 Miami, FL 33137 (844) ANATRA-1

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqr-codes.io/mVOmE7Updated_image60_2_V2.jpg, Updated_image30_2_V2.jpg, Updated_image30_1_V2.jpg, Updated_image60_1_V2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83641-001-01Anatra30 in 1 BOTTLE, PLASTICTABLET303
83641-001-02Anatra60 in 1 BOTTLE, PLASTICTABLET603

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83641-00183641-001-01, 83641-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-01-13full-release2026-06-01 00:52:34

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
AnatraANAS BARBARIAEAnatra LLC4562fa87-ed88-42fb-b530-e600aea351d92025-10-07WarningsExact identifier
ndc (package): 83641-001-01
ndc (package): 83641-001-02
ndc (product): 83641-001
ndc11 (package): 83641000102
ndc11 (package): 83641000101
spl id: 4097d2e5-5d3f-b62a-e063-6294a90a882f
spl set id: 4562fa87-ed88-42fb-b530-e600aea351d9

Reported adverse events (FAERS/openFDA)#

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