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Name:Nu Skin Epoch
Manufacturer:Alberto-culver Usa Inc.
Category:Over-the-counter (OTC) Marketed Drugs


Epoch® Antiseptic Hand Sanitizer

NU SKIN EPOCH - alcohol gel 
Alberto-Culver USA Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Epoch® Antiseptic
Hand Sanitizer

Active Ingredient

SD Alcohol 40-B (62%)

Usage

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

Warnings

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

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

Inactive Ingredients

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

Questions?

1-888-742-7626

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

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

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 (Back)

NU SKIN EPOCH 
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:12488-1800
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (Alcohol) Alcohol 61.9937 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water  
Polyoxyl 40 Hydrogenated Castor Oil  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:12488-1800-1 100 mL in 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333 06/01/2009

Labeler - Alberto-Culver USA Inc. (021679448)
Establishment
Name Address ID/FEI Operations
Alberto-Culver USA Inc. 021679448 ANALYSIS, MANUFACTURE

Revised: 12/2009 Alberto-Culver USA Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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