Glauco

Manufacturer
Newton Laboratories, Inc.
Effective date
2020-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:13:48

Label at a glance#

ProductGlauco
Active ingredientACONITUM NAPELLUS, ATROPA BELLADONNA, CAUSTICUM, CINCHONA OFFICINALIS BARK, COLCHICUM AUTUMNALE BULB, EUPHRASIA STRICTA, GELSEMIUM SEMPERVIRENS ROOT, STRYCHNOS NUX-VOMICA SEED, OSMIUM, PHOSPHORUS, PHYSOSTIGMA VENENOSUM SEED, TOXICODENDRON PUBESCENS LEAF, SPIGELIA ANTHELMIA, GOLD
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for symptoms such as blurred vision and red eyes..

DOSAGE & ADMINISTRATION SECTION

Directions: Adults take 6 drops by mouth one to four times daily or as directed by a health professional. Use in conjunction with eye exam.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Aconitum napellus 15x, Aurum metallicum 15x, Belladonna 15x, Causticum 15x, Cinchona officinalis 15x, Colchicum autumnale 15x, Euphrasia officinalis 15x, Gelsemium sempervirens 15x, Nux vomica 15x, Osmium metallicum 15x, Phosphorus 15x, Physostigma venenosum 15x, Rhus toxicodendron 15x, Spigelia anthelmia 15x.

OTC - PURPOSE SECTION

Formulated for symptoms such as blurred vision and red eyes.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net - Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-4810-1Glauco30 mL in 1 BOTTLE, GLASSLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-4810GLAUCO (ACONITUM NAPELLUS, AURUM METALLICUM, BELLADONNA, CAUSTICUM, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, NUX VOMICA, OSMIUM METALLICUM, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, RHUS TOXICODENDRON, SPIGELIA ANTHELMIA.) LIQUID [NEWTON LABORATORIES, INC.]2Current NDC, Legacy NDC, 1 package rows20201204_9a6394e7-14ed-ced1-e053-2995a90aeb88.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-481055714-4810-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
GlaucoACONITUM NAPELLUS, AURUM METALLICUM, BELLADONNA, CAUSTICUM, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, NUX VOMICA, OSMIUM METALLICUM, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, RHUS TOXICODENDRON, SPIGELIA ANTHELMIA.Newton Laboratories, Inc.9a6394e7-14ed-ced1-e053-2995a90aeb882020-12-03WarningsExact identifier
ndc (package): 55714-4810-1
ndc (product): 55714-4810
ndc11 (package): 55714481001
spl id: b5943091-6c09-08d3-e053-2995a90ac912
spl set id: 9a6394e7-14ed-ced1-e053-2995a90aeb88

Reported adverse events (FAERS/openFDA)#

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