FDA.reportPublic FDA data

INNER BEAUTY GEL

Manufacturer
MISMIZBio Inc.
Effective date
2018-03-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:56

Label at a glance#

ProductINNER BEAUTY GEL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INNER BEAUTY GELINNER BEAUTY GEL

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - WHEN USING SECTION

OTC - STOP USE SECTION

OTC - PURPOSE SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - ASK DOCTOR SECTION

INDICATIONS & USAGE SECTION

OTC - DO NOT USE SECTION

OTC - ACTIVE INGREDIENT SECTION

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
2ee8a2ab-68f9-45f5-8e16-b382e1af7d34Product name120200618
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71984-4200-12022-01-28C16284748780-1d6a99b39-b73c-a426-e053-dadaa90af4c267a90218-7de4-39f1-e053-2a91aa0a732b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71984-4200-1INNER BEAUTY GEL4.2 mL in 1 APPLICATORSOLUTION4.21
71984-4200-1INNER BEAUTY GEL8 in 1 BOXSOLUTION81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71984-4200INNER BEAUTY GEL (GLYCERIN) SOLUTION [MISMIZBIO INC.]12 package rows20180320_67a90218-7de4-39f1-e053-2a91aa0a732b.zip

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71984-420071984-4200-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
COPTIS CHINENSIS ROOTCXS4LJR7ELINGR
POLYGLYCERYL-10 LAURATEMPJ2Q8WI8GINGR
MAGNOLIA KOBUS BARK54LVP49595INGR
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SINGR
ZANTHOXYLUM PIPERITUM WHOLEY8IKP41338INGR
PULSATILLA KOREANA WHOLE5R35881OBKINGR
ROSA CENTIFOLIA FLOWERCS4TE8FF7OINGR
ADENOSINEK72T3FS567INGR
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NINGR
HYALURONIC ACIDS270N0TRQYINGR
CANANGA ODORATA FLOWER76GTF6Z97MINGR
SOYBEAN GERMJBW2VHD14MINGR
WATER059QF0KO0RINGR
BUTYLENE GLYCOL3XUS85K0RAINGR
PROPANEDIOL5965N8W85TINGR
PUNICA GRANATUM WHOLEO2ZTS50U5EINGR
PENTYLENE GLYCOL50C1307PZGINGR
HAMAMELIS VIRGINIANA FLOWER WATER222MYC9QUVINGR
KONJAC MANNAN36W3E5TAMGINGR
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXINGR
PAEONIA SUFFRUTICOSA ROOT7M7E9A2C8JINGR
ROSA DAMASCENA FLOWER OIL18920M3T13INGR
LACTITOLL2B0WJF7ZYINGR
GLYCYRRHIZA GLABRA2788Z9758HINGR
USNEA BARBATAD6DVA9TCAPINGR
GLYCERINPDC6A3C0OXINGR
CENTELLA ASIATICA7M867G6T1UINGR
LACTIC ACID33X04XA5ATINGR
ALOE VERA LEAFZY81Z83H0XINGR

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
67a90218-7de5-39f1-e053-2a91aa0a732b67a90218-7de4-39f1-e053-2a91aa0a732b2018-03-18Exact identifier
spl id: 67a90218-7de5-39f1-e053-2a91aa0a732b
spl set id: 67a90218-7de4-39f1-e053-2a91aa0a732b

Reported adverse events (FAERS/openFDA)#

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