Angiplex

Manufacturer
Seroyal USA | SAN'UP
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:25

Label at a glance#

ProductAngiplex
Active ingredientARISAEMA TRIPHYLLUM ROOT, ACONITUM NAPELLUS, APIS MELLIFERA, ATROPA BELLADONNA, PHYTOLACCA AMERICANA ROOT, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, MERCURIUS SOLUBILIS
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Each tablet contains:
Aconitum napellus (Aconite) Whole Plant 8X
Apis mellifica (Honey bee) 8X
Arum triphyllum (Indian turnip) Underground Parts 4X
Belladonna (Deadly nightshade) Whole Plant 8X
(< 1.25 x 10-10 % alkaloids, calculated)
Kalium bichromicum (Potassium bichromate) 10X
Lachesis mutus (Bushmaster) Venom 10X
Mercurius solubilis (Hahnemann's soluble mercury) 10X
Phytolacca decandra (Pokeweed) Root 8X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with
sore throat

dry throat

WARNINGS SECTION

Warnings

Sore throat warning: Severe or persistent sore throat or sore
throat accompanied by high fever, headache, nausea, and
vomiting may be serious. Consult physician promptly. Do not use
more than 2 days or administer to children under 3 years of age
unless directed by physician.
Stop use and ask a doctor if symptoms continue to persist
after three days of use or are accompanied by a fever.
Do not use if you have ever had an allergic reaction to this
product or any of its ingredients.
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 - DO NOT USE SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical
help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Lactose monohydrate (milk), magnesium stearate, sodium carboxymethylcellulose, xylitol

OTHER SAFETY INFORMATION

Other information

Do not use if the blister pack has been tampered with.

Store in a cool, dry place.

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and adolescents (12 years and older): At the first sign of symptoms, dissolve one tablet under the tongue every
half hour to one hour. When symptoms subside, decrease frequency to every four hours. Once the symptoms are gone,
continue taking one tablet daily for three more days.

Children (under 12 years): Take under the direction of your healthcare practitioner.

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of symptoms associated with
sore throat

dry throat

Directions

Adults and adolescents (12 years and older): At the first sign of symptoms, dissolve one tablet under the tongue every
half hour to one hour. When symptoms subside, decrease frequency to every four hours. Once the symptoms are gone,
continue taking one tablet daily for three more days.

Children (under 12 years): Take under the direction of your healthcare practitioner.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-122962106-1229

NDC 62106-1229-3

UNDA plex

ANGIPLEX
Homeopathic Preparation

For the temporary relief of sore throat and dry throat.

30 Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1229-3Angiplex30 in 1 BLISTER PACKTABLET305
62106-1229-3Angiplex1 in 1 BOXTABLET15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1229ANGIPLEX (ARUM TRIPHYLLUM, ACONITUM NAPELLUS, APIS MELLIFICA, BELLADONNA, PHYTOLACCA DECANDRA, KALI BICHROMICUM, LACHESIS MUTUS, MERCURIUS SOLUBILIS) TABLET [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20221110_0d04b1a0-6c43-5f25-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD2
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z2
ARISAEMA TRIPHYLLUM ROOTACTIVE INGREDIENTDM64K844DM2
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H2
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I2
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G22
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG2
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM2
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD2
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z2
ARISAEMA TRIPHYLLUM ROOTACTIVE MOIETYDM64K844DM2
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H2
DICHROMATE IONACTIVE MOIETY9LKY4BFN2V2
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I2
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G22
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG2
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS3112
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5X2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I302
XYLITOLINACTIVE INGREDIENTVCQ006KQ1E2

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-122962106-1229-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
4 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
4 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / ORAL280 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / BUCCAL4 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / ORAL280 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / BUCCAL4 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
AngiplexARUM TRIPHYLLUM, ACONITUM NAPELLUS, APIS MELLIFICA, BELLADONNA, PHYTOLACCA DECANDRA, KALI BICHROMICUM, LACHESIS MUTUS, MERCURIUS SOLUBILISSeroyal USA0d04b1a0-6c43-5f25-e054-00144ff8d46c2022-11-09WarningsExact identifier
ndc (package): 62106-1229-3
ndc (product): 62106-1229
ndc11 (package): 62106122903
spl id: ed11e5b0-cdb3-1f9a-e053-2995a90a0f16
spl set id: 0d04b1a0-6c43-5f25-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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