FDA.reportPublic FDA data

Nu Skin Epoch

Manufacturer
Alberto-Culver USA Inc.
Effective date
2009-12-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:03

Label at a glance#

ProductNu Skin Epoch
Active ingredientAlcohol
Label structure8 sections

Dosage and administration

Place a teaspoon of product in one hand. Spread on both hands, applying liberally. Rub gently until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

SD Alcohol 40-B (62%)

Usage

INDICATIONS & USAGE SECTION

Disinfects and provides protection by killing 99.99% of the most common harmful germs and bacteria.

Warnings

WARNINGS SECTION

For external use only. Keep out of reach of children. Keep out of eyes. Discontinue use if irritation develops. If condition persists for more than 72 hours consult a physician. Flammable, keep away from fire or flame.

Directions

DOSAGE & ADMINISTRATION SECTION

Place a teaspoon of product in one hand. Spread on both hands, applying liberally. Rub gently until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Lavandula Angustifolia (Lavender) Oil, Lonicera Japonica (Honeysuckle) Flower Extract, PEG-40 Hydrogenated Castor Oil, Carbomer, Aminomethyl Propanol, Fragrance (Parfum), Chlorphenesin.

Questions?

OTC - QUESTIONS SECTION

1-888-742-7626

SPL UNCLASSIFIED SECTION

Mfd. in the U.S.A exclusively for
NSE Products, Inc., Provo, UT 84601

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

epoch®

with Lavender,
Honeysuckle Extract,
and Chlorphenesin

Antiseptic

Hand Sanitizer

100 ml e (3.4 fl. oz.)

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Front)
PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Front)
PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Back)
PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Back)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020119isopropyl alcohol 62 % Topical GelPSN1
1020119isopropyl alcohol 0.62 ML/ML Topical GelSCD1
1020119isopropyl alcohol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
12488-1800-12020-01-31C16284748780-19d75b9d0-e026-f424-e053-dadaa90a57ceEpoch ® Antiseptic Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12488-1800-1Nu Skin Epoch100 mL in 1 BOTTLE, PLASTICGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12488-1800NU SKIN EPOCH (ALCOHOL) GEL [ALBERTO-CULVER USA INC.]1Legacy NDC, 1 package rows20091219_741afc13-5f33-4c9d-90ab-7b0cda69a0df.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M1
AlcoholACTIVE MOIETY3K9958V90M1
Polyoxyl 40 Hydrogenated Castor OilINACTIVE INGREDIENT7YC686GQ8F1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12488-180012488-1800-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
Polyoxyl 40 Hydrogenated Castor Oil7YC686GQ8FIACT

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
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FCAPSULE, COATED / ORAL101.25 mgExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FCREAM / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FTABLET, EXTENDED RELEASE / ORAL50 mgExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FTABLET / ORAL120 mgExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FSOLUTION / OPHTHALMIC3 mgExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FSOLUTION / DENTAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FSOLUTION / ORAL3240 mgExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FSOLUTION/ DROPS / OPHTHALMIC0.53 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
Polyoxyl 40 Hydrogenated Castor OilPOLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FCAPSULE / ORAL3319 mgExact identifier — unii candidate
9 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
aba16eab-dfe7-4370-bf7a-43059ccccf0d741afc13-5f33-4c9d-90ab-7b0cda69a0df2009-12-14WarningsExact identifier
spl id: aba16eab-dfe7-4370-bf7a-43059ccccf0d
spl set id: 741afc13-5f33-4c9d-90ab-7b0cda69a0df

Reported adverse events (FAERS/openFDA)#

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