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Name:Nuglow Daytime Therapy With Spf 15
Manufacturer:G.s. Cosmeceutical Usa, Inc.
Category:Over-the-counter (OTC) Marketed Drugs


NuGLOW®

NUGLOW  DAYTIME THERAPY WITH SPF 15 - avobenzone, octinoxate and zinc oxide cream 
G.S. COSMECEUTICAL 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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NuGLOW®

DIRECTIONS

After cleansing, apply liberally to face daily. Apply evenly before sun exposure. Reapply as needed after towel drying, swimming or perspiring.

Children under 6 months: ask a doctor.

WARNINGS

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

QUESTIONS?

1-866-605-9510 or visit www.nuglowskincare.com.

Daytime Therapy With SPF15

ACTIVE INGREDIENTS

Avobenzone 1.0%, Octinoxate 7.0%, Zinc Oxide 4.0%.

INACTIVE INGREDIENTS

Aqua (Water), Caprylic/Capric Triglyceride, Glyceryl Stearate SE, Butyrospermum Parkii (Shea Butter), Polysorbate 60, Cetyl Alcohol, Dimethicone, Cetyl Ricinoleate, Stearyl Alcohol, Persea Gratissima (Avocado) Oil, Glycerin, Sodium Hyaluronate, Camellia Oleifera (Green Tea) Leaf Extract, Chrondrus Crispus (Carrageenan), Sodium PCA, Xanthan Gum, Tocopheryl Acetate, Ascorbic Acid, Lactic Acid, Glucose, Triethoxycaprylylsilane, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol.

For expiration date, see bottom of jar.

Made in the U.S.A. for NuGlow, Los Angeles, CA 90049

Reorder# 70825
Rev 8/10

PRINCIPAL DISPLAY PANEL - 34g Jar Label

NuGlow®

Daytime Therapy
With SPF15

Net Weight 1.2 Oz./34g e

PRINCIPAL DISPLAY PANEL - 34g Jar Label

NUGLOW   DAYTIME THERAPY WITH SPF 15
avobenzone, octinoxate, and zinc oxide cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:65113-8503
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOBENZONE (AVOBENZONE) AVOBENZONE 1 g  in 100 g
OCTINOXATE (OCTINOXATE) OCTINOXATE 7 g  in 100 g
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE 4 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER  
CETYL ALCOHOL  
DIMETHICONE  
STEARYL ALCOHOL  
AVOCADO OIL  
GLYCERIN  
CAMELLIA OLEIFERA LEAF  
XANTHAN GUM  
ASCORBIC ACID  
LACTIC ACID  
TRIETHOXYCAPRYLYLSILANE  
PHENOXYETHANOL  
CAPRYLYL GLYCOL  
HEXYLENE GLYCOL  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:65113-8503-3 34 g in 1 JAR None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part352 10/15/2010

Labeler - G.S. COSMECEUTICAL USA, INC. (017014734)
Establishment
Name Address ID/FEI Operations
G.S. COSMECEUTICAL USA, INC. 017014734 MANUFACTURE

Revised: 02/2011 G.S. COSMECEUTICAL USA, INC.



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


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