FDA.reportPublic FDA data

BOTHROPS LANCEOLATUS

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:48:53

Label at a glance#

ProductBOTHROPS LANCEOLATUS
Active ingredientBOTHROPS ATROX VENOM
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

BOTHROPS LANCEOLATUS 200K GR

BOTHROPS LANCEOLATUS 30K GR

BOTHROPS LANCEOLATUS 5CH GR

OTC - PURPOSE SECTION

Indications

Helps to support visual health

WARNINGS SECTION

Warning:
If pregnant or breastfeeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Lactose,
sucrose.

DOSAGE & ADMINISTRATION SECTION

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

OTC - QUESTIONS SECTION

QUESTIONS? 1-888-737-6925.

INDICATIONS & USAGE SECTION

Indications

Helps to support visual health

Directions
Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
Children: Take three granules and follow adult directions.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-665362106-6653

UNDA
Do not use if label perforation is broken
Homeopathic Remedy
NDC : 62106-6653-4
BOTHROPS LANCEOLATUS
Yellow viper
140 granules
Indications

Helps to support visual health

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
62106-665362106-6653-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTOSEJ2B2A4N98GIACT
SUCROSEC151H8M554IACT
BOTHROPS ATROX VENOMK0Q6REZ9JCACTIB

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
075fc7c9-7b4a-b9c3-e063-6394a90a926e2f0c0aa8-d06b-4f48-e054-00144ff88e882023-10-10WarningsExact identifier
spl set id: 2f0c0aa8-d06b-4f48-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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