FDA.reportPublic FDA data

FOREVER LASTING PRECIOUS ESSENTIAL WATER

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:34

Label at a glance#

ProductFOREVER LASTING PRECIOUS ESSENTIAL WATER
Active ingredientGLYCERIN
Label structure8 sections

Indications and uses

How to Use: After washing, pump out a small amount and apply gently over face.

Dosage and administration

How to Use: After washing, pump out a small amount and apply gently over face.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: GLYCERIN 20.42%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
WATER, MANNAN, PANTHENOL, BUTYLENE GLYCOL, PEG-60 HYDROGENATED CASTOR OIL, 1,2-HEXANEDIOL, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, PHENOXYETHANOL, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, ARCTIUM LAPPA ROOT EXTRACT, PHELLINUS LINTEUS EXTRACT, ALLANTOIN, ETHYLHEXYLGLYCERIN, HELICHRYSUM ITALICUM FLOWER WATER, PROPYLENE GLYCOL, PORTULACA OLERACEA EXTRACT, PUERARIA THUNBERGIANA ROOT EXTRACT, CNIDIUM OFFICINALE ROOT EXTRACT, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, PAEONIA LACTIFLORA ROOT EXTRACT, JUNIPERUS COMMUNIS FRUIT EXTRACT, TILIA VULGARIS FLOWER EXTRACT, HYDROLYZED SOY PROTEIN, SOLUBLE COLLAGEN, ADENOSINE, FRAGRANCE, ALOE BARBADENSIS LEAF JUICE, SODIUM HYALURONATE, ANTHEMIS NOBILIS FLOWER WATER, HAMAMELIS VIRGINIANA FLOWER WATER, HYDROGENATED LECITHIN, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER WATER, MELISSA OFFICINALIS FLOWER/LEAF/STEM WATER, PVM/MA COPOLYMER, PENTYLENE GLYCOL, SODIUM POLYACRYLATE, XANTHAN GUM, CAPROOYL TETRAPEPTIDE-3, DEXTRAN

PURPOSE

OTC - PURPOSE SECTION

Purpose:
Toner for treating premature aging which infuses an eternal youth into the skin with the revitalizing ingredients of Immortelle Flower Water and 6 organic herbal extracts.
It stimulates collagen production to fill wrinkles and promote a youthful elasticity.

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 washing, pump out a small amount and apply gently over face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: After washing, pump out a small amount and apply gently over 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
51346-183-012021-07-14C16284748780-19d75b9d1-0ac2-f424-e053-dadaa90a57ce81385faf-62f7-4962-89b6-235df175f583
51346-183-012020-01-31C16284748780-19d75b9d1-0ac2-f424-e053-dadaa90a57ce81385faf-62f7-4962-89b6-235df175f583

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
ALLANTOININACTIVE INGREDIENT344S277G0Z1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
PANTHENOLINACTIVE INGREDIENTWV9CM0O67Z1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-18351346-183-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIM
WATER059QF0KO0RIACT
PANTHENOLWV9CM0O67ZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
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 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
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
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
97f83e53-4533-43a4-8f88-b53d17e8502781385faf-62f7-4962-89b6-235df175f5832021-07-13WarningsExact identifier
spl set id: 81385faf-62f7-4962-89b6-235df175f583

Reported adverse events (FAERS/openFDA)#

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