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Name:Neutracetttattoo
Manufacturer:Advanced Biomedics Inc
Category:Over-the-counter (OTC) Marketed Drugs


TUBE LABEL

NEUTRACETT TATTOO - allantoin and glycerin gel 
ADVANCED BIOMEDICS 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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TUBE LABEL

Inactive Ingredients: Water (Aqua), Neutracett Complex (Hyaluronic Acid, DL Panthenol), PPG-5-Ceteth-20, Ammonium Acryloyldimethyltaurate/VP Copolymer, Phenoxyethanol, Chlorphenesin, Benzoic Acid.

Active ingredients/Purpose

Allantoin 0.5%    Skin Protectant

Glycerin 5.0%    Skin Protectant

Ask a doctor before use if you have: *serious burns * deep or puncture wounds * animal bites

Questions? 800-833-4164

www.neutracett.com Patents Pending

Do not use: *if you are allergic to any of the ingredients *avoid contact with the eyes

Stop use and ask a doctor: * if condition worsens or does not improve after 7 days * if rash or other allergic reactions occur

Uses: Soothes, protects and eases skin trauma for tattoo application or removal.

Warnings: For external use only.

Directions: Gently clean area with mild cleanser. Apply gel to entire area 3-4 times per day or as directed. May be covered with sterile bandage. See website for more information.

Neutracett

Aid 4-Healing

Skin Recovery Treatment

For Tattoo, tattoo removal

All natural / won’t stain

Tattoo Care Neutracett Artwork-LBL


NEUTRACETT  TATTOO
allantoin glycerin gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:51435-002
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (ALLANTOIN) ALLANTOIN 0.5 mg  in 0.1 g
GLYCERIN (GLYCERIN) GLYCERIN 50 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER  
HYALURONIC ACID  
PANTHENOL  
PPG-5-CETETH-20  
PHENOXYETHANOL  
CHLORPHENESIN  
BENZOIC ACID  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51435-002-01 28.3 g in 1 TUBE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 05/28/2010

Labeler - ADVANCED BIOMEDICS INC (023307026)
Registrant - ADVANCED BIOMEDICS INC (023307026)
Establishment
Name Address ID/FEI Operations
COSMETIC ENTERPRISES LTD 017701475 manufacture

Revised: 08/2010 ADVANCED BIOMEDICS INC



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


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