Elberry Up

Manufacturer
Nartex Laboratorios Homeopaticos SA DE CV
Effective date
2024-12-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:46:36

Label at a glance#

ProductElberry Up
Active ingredientSAMBUCUS NIGRA FLOWERING TOP, BRYONIA ALBA ROOT, SULFUR
Label structure12 sections

Indications and uses

Temporarily relieves discomforting symptoms such as: runny nose sore throat coughing sneezing and nasal congestion Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA, and product has not been clinically tested.

Dosage and administration

- adults and children 4 years of age and older: take 2 tablets every 6 hours. - children under 4 years of age, consult a physician.

Storage and handling

- store in a cool dry place. - do not use if blister pack is broken.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sambucus Nigra 6x HPUS*

Bryonia 6x HPUS*

Sulphur 12x HPUS*

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. "X" is a homeopathic dilution. See www.nartexlabsusa.com for more information.

Purpose

OTC - PURPOSE SECTION

Sambucus Nigra 6x HPUS*..............Nasal Congestion

Bryonia 6x HPUS*..............Nasal Congestion and antitussive

Sulphur 12x HPUS*..............Nasal Congestion and anti-inflammatory

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves discomforting symptoms such as:

  • runny nose
  • sore throat
  • coughing
  • sneezing and nasal congestion

Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA, and product has not been clinically tested.

OTC - DO NOT USE SECTION

Do not useif you have if you have an allergy or hypersensitivity to the components of the formula or have had a prior reaction to this product.

OTC - STOP USE SECTION

Stop use and ask a doctor if

- condition worsens

- symptoms persist for more than 7 days or clear up and occur again within a few days.

- rash develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

- adults and children 4 years of age and older: take 2 tablets every 6 hours.

- children under 4 years of age, consult a physician.

Other Information

STORAGE AND HANDLING SECTION

- store in a cool dry place.

- do not use if blister pack is broken.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Gelatin, lactose, magnesium stearate, potato starch, purified water, sodum benzoate, talc

Questions or Comments?

OTC - QUESTIONS SECTION

informacion@nartexlabs.com or call 1-877-248-1970 between 9am and 5pm CST. Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States, and are therefore non-toxic and have no known side effects. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by FDA , and product has not been clinically tested.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
34666-31134666-311-01

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

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
2918bd69-79ff-cf25-e063-6394a90a8443ae6db3ca-740b-1ddf-e053-2995a90a24c72024-12-12WarningsExact identifier
spl id: 2918bd69-79ff-cf25-e063-6394a90a8443
spl set id: ae6db3ca-740b-1ddf-e053-2995a90a24c7

Reported adverse events (FAERS/openFDA)#

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