Miraculous

Manufacturer
Qingdao Aolixin Sanitary Products Co., Ltd.
Effective date
2022-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:17:20

Label at a glance#

ProductMiraculous
Active ingredientANGELICA SINENSIS ROOT, PLATYCODON GRANDIFLORUS ROOT
Label structure12 sections

Indications and uses

For the temporary relief of symptoms due to inflammation.

Dosage and administration

For those under 60 years old, take one package (9g) three times a day, two hours after breakfast and lunch, and one package (9g) 30 minutes before going to bed It is recommended to eat one package (9g) 2 hours after breakfast and one package (9g) 30 minutes before going to bed.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

ANGELICA SINENSIS ROOT 4%

PLATYCODON GRANDIFLOROUS ROOT 5%

OTC - PURPOSE SECTION

Detoxification

Anti inflammation

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms due to inflammation.

Warnings

WARNINGS SECTION

Do not take more than specified amount.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Stop use and ask a doctor

OTC - STOP USE SECTION

if symptoms of discomfort worsen.

if you develop severe red spots or itching.

Do not use

OTC - DO NOT USE SECTION

when taking painkillers and laxatives.

When using

OTC - WHEN USING SECTION

it is normal to have diarrhea for 2-3 days.

Directions

DOSAGE & ADMINISTRATION SECTION

For those under 60 years old, take one package (9g) three times a day, two hours after breakfast and lunch, and one package (9g) 30 minutes before going to bed It is recommended to eat one package (9g) 2 hours after breakfast and one package (9g) 30 minutes before going to bed.

Other Information

OTHER SAFETY INFORMATION

It is recommended to go to a regular hospital for check up after 3 months. Avoid cold and avoid spicy food while taking it.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Rhizome sparganii, Subprostrate sophora, The root of red-rooted salvia, Radix scrophulariae, The root of straight ladybel, Codonopsis pilosula, Atractylodes macrocephalal, Radix Paeoniae Rubra, Tulip、Baikal Skullcap, Poria cocos, Rhizoma Curcumae, Zhebeinine, Semen Impatientis, Dandelion, The root bark of the peony tree, Cinnamon, Ground beetle, Squirrel's droppings, Carthamus, Cordyceps sinensis, Squama Manis, Radix Aucklandiae, Corydalis, Leeches, Polygonum wilfordii

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Miraculous LabelMiraculous Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82672-302-012023-07-28C16284748780-10191ceaa-6f7b-198a-e063-dbdaa90aec3eMiraculous

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82672-302-01Miraculous9 g in 1 BAGPOWDER91

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82672-302MIRACULOUS (PLATYCODON GRANDIFLORUS ROOT, ANGELICA SINENSIS ROOT) POWDER [QINGDAO AOLIXIN SANITARY PRODUCTS CO., LTD.]1Legacy NDC, 1 package rows20220422_dce4236f-6c1a-21b6-e053-2995a90a29fa.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82672-30282672-302-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
dce4236f-6c1b-21b6-e053-2995a90a29fadce4236f-6c1a-21b6-e053-2995a90a29fa2022-04-17WarningsExact identifier
spl id: dce4236f-6c1b-21b6-e053-2995a90a29fa
spl set id: dce4236f-6c1a-21b6-e053-2995a90a29fa

Reported adverse events (FAERS/openFDA)#

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