FDA.reportPublic FDA data

BETTER THAN NATURE SKIN SOFTNER

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:47

Label at a glance#

ProductBETTER THAN NATURE SKIN SOFTNER
Active ingredientGLYCERIN
Label structure8 sections

Indications and uses

How to Use: After cleansing, apply an appropriate amount on a cotton pad and gently wipe your face.

Dosage and administration

How to Use: After cleansing, apply an appropriate amount on a cotton pad and gently wipe your face.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: GLYCERIN 20%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
CENTAUREA CYANUS FLOWER WATER, BUTYLENE GLYCOL, BETAINE, PENTYLENE GLYCOL, AMARANTHUS CAUDATUS SEED EXTRACT, ULMUS DAVIDIANA ROOT EXTRACT, PEG-40 HYDROGENATED CASTOR OIL, ARCTIUM LAPPA ROOT EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, ANTHEMIS NOBILIS FLOWER WATER, CAMELLIA SINENSIS LEAF WATER, CITRUS AURANTIUM DULCIS (ORANGE) FRUIT WATER,
EPILOBIUM ANGUSTIFOLIUM FLOWER/LEAF/STEM EXTRACT, HAMAMELIS VIRGINIANA FLOWER WATER, HELICHRYSUM ITALICUM FLOWER WATER, HIBISCUS ESCULENTUS FRUIT EXTRACT, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER WATER, LINUM USITATISSIMUM (LINSEED) SEED EXTRACT, MELISSA OFFICINALIS FLOWER/LEAF/STEM WATER, PORTULACA OLERACEA EXTRACT, ROSA DAMASCENA FLOWER WATER, SODIUM CITRATE, TILIA VULGARIS FLOWER EXTRACT, GANODERMA LUCIDUM (MUSHROOM) EXTRACT, GRIFOLA FRONDOSA EXTRACT, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT, PHELLINUS LINTEUS EXTRACT, SPARASSIS CRISPA EXTRACT, DIPOTASSIUM GLYCYRRHIZATE,
ETHYLHEXYLGLYCERIN, PHENOXYETHANOL, CITRIC ACID, FRAGRANCE, DISODIUM EDTA

PURPOSE

OTC - PURPOSE SECTION

Purpose: A mild toner more natural than nature.

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use: After cleansing, apply an appropriate amount on a cotton pad and gently wipe your face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: After cleansing, apply an appropriate amount on a cotton pad and gently wipe your face.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-117-012021-07-14C16284748780-19d75b9d0-87dc-f424-e053-dadaa90a57ceb852d2f9-2893-4655-9d4e-e3d6462a074e
51346-117-012020-01-31C16284748780-19d75b9d0-87dc-f424-e053-dadaa90a57ceb852d2f9-2893-4655-9d4e-e3d6462a074e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
BETAINEINACTIVE INGREDIENT3SCV180C9W1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
ETHYLHEXYLGLYCERININACTIVE INGREDIENT147D247K3P1
PENTYLENE GLYCOLINACTIVE INGREDIENT50C1307PZG1
PHENOXYETHANOLINACTIVE INGREDIENTHIE492ZZ3T1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-11751346-117-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIM
BUTYLENE GLYCOL3XUS85K0RAIACT
BETAINE3SCV180C9WIACT
PENTYLENE GLYCOL50C1307PZGIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TCREAM / TOPICAL57 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TAEROSOL, FOAM / TOPICAL72 mgExact identifier — unii candidate
6 equally ranked IID candidates
PHENOXYETHANOLPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
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
acc4c963-4424-4f0e-9d66-ef0df66db8b3b852d2f9-2893-4655-9d4e-e3d6462a074e2021-07-13WarningsExact identifier
spl set id: b852d2f9-2893-4655-9d4e-e3d6462a074e

Reported adverse events (FAERS/openFDA)#

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