FDA.reportPublic FDA data

SELLA CLASSIC NATURAL GOLD SERUM

Manufacturer
Sella Natural Cosmetics Co.,Ltd.
Effective date
2015-02-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:39

Label at a glance#

ProductSELLA CLASSIC NATURAL GOLD SERUM
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerine


INACTIVE INGREDIENT SECTION

water, butylene glycol, allantoin, panthenol etc


OTC - PURPOSE SECTION

skin protectant
skin humectant


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply to the skin and rub gently


WARNINGS SECTION

・Stop using the product when you have skin problems or the product disagrees with your skin
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.


DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69603-0201-12020-01-31C16284748780-19d75b9d1-0909-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69603-0201-1SELLA CLASSIC NATURAL GOLD SERUM30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69603-0201SELLA CLASSIC NATURAL GOLD SERUM (GLYCERIN) LIQUID [SELLA NATURAL COSMETICS CO.,LTD.]1Legacy NDC, 1 package rows20150211_8341c0b3-338f-4a2e-862d-a2951a0dc68c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
ALLANTOININACTIVE INGREDIENT344S277G0Z1
PANTHENOLINACTIVE INGREDIENTWV9CM0O67Z1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
69603-020169603-0201-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIB
WATER059QF0KO0RIACT
PANTHENOLWV9CM0O67ZIACT
ALLANTOIN344S277G0ZIACT

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 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALLANTOINALLANTOIN344S277G0ZGEL / TOPICAL8 mgExact identifier — unii candidate

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
d5ed8cab-384f-4eb3-ac51-d6824325950f8341c0b3-338f-4a2e-862d-a2951a0dc68c2015-02-11WarningsExact identifier
spl id: d5ed8cab-384f-4eb3-ac51-d6824325950f
spl set id: 8341c0b3-338f-4a2e-862d-a2951a0dc68c

Reported adverse events (FAERS/openFDA)#

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