FDA.reportPublic FDA data

FRESH AFTER VACANCE BODY SOOTHING

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:36

Label at a glance#

ProductFRESH AFTER VACANCE BODY SOOTHING
Active ingredientGlycerin
Label structure8 sections

Indications and uses

How to Use: Apply to dry, irritated skin as often as needed to soothe the skin.

Dosage and administration

How to Use: Apply to dry, irritated skin as often as needed to soothe the skin.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Glycerin 20%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Dipropylene Glycol, Betaine, Pentylene Glycol, Phenoxyethanol, Biosaccharide Gum-1, Carbomer, Arginine, PEG-60 Hydrogenated Castor Oil, Octyldodeceth-16, Fragrance(Parfum), Disodium EDTA, Butylene Glycol, Gaultheria Procumbens (Wintergreen) Leaf Extract, Propylene Glycol, Mimosa Tenuiflora Bark Extract, Sorbitol, Sodium Hydroxide, Citric Acid, Ethylhexylglycerin

PURPOSE

OTC - PURPOSE SECTION

Purpose: Provides moisture to dry skin without leaving any sticky residue behind. It soothes scorched, sensitive skin and provides a refreshing sensation as it is quickly absorbed into the skin.

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: Apply to dry, irritated skin as often as needed to soothe the skin.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: Apply to dry, irritated skin as often as needed to soothe the skin.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809344264091GTIN-13: 8809344264091
EAN-13: 8809344264091
GTIN storage (14 digits): 08809344264091		fresh after vacance body soothing carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-171-012021-07-09C16284748780-19d75b9cf-d7b4-f424-e053-dadaa90a57cea6d4c5a0-8276-4d02-9573-b439be2780a4
51346-171-012020-01-31C16284748780-19d75b9cf-d7b4-f424-e053-dadaa90a57cea6d4c5a0-8276-4d02-9573-b439be2780a4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX1
GlycerinACTIVE MOIETYPDC6A3C0OX1
BetaineINACTIVE INGREDIENT3SCV180C9W1
Dipropylene GlycolINACTIVE INGREDIENTE107L85C401
Pentylene GlycolINACTIVE INGREDIENT50C1307PZG1
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
51346-17151346-171-01

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
Water059QF0KO0RIACT
Dipropylene GlycolE107L85C40IACT
Betaine3SCV180C9WIACT
Pentylene Glycol50C1307PZGIACT
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 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TAEROSOL / TOPICAL1.05 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 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
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TCREAM, AUGMENTED / TOPICAL10 mgExact identifier — unii candidate
6 equally ranked IID candidates
PhenoxyethanolPHENOXYETHANOLHIE492ZZ3TLOTION / TOPICAL1 %w/wExact identifier — unii candidate
6 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
b9bc9a95-07bd-43a3-a3c1-1bd283b22be2a6d4c5a0-8276-4d02-9573-b439be2780a42021-07-08WarningsExact identifier
spl set id: a6d4c5a0-8276-4d02-9573-b439be2780a4

Reported adverse events (FAERS/openFDA)#

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