NEUTRACETT TATTOO- allantoin glycerin gel

NEUTRACETT by

Drug Labeling and Warnings

NEUTRACETT by is a Otc medication manufactured, distributed, or labeled by ADVANCED BIOMEDICS INC, COSMETIC ENTERPRISES LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

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

ACTIVE INGREDIENT

Active ingredients/Purpose

Allantoin 0.5%    Skin Protectant

Glycerin 5.0%    Skin Protectant

ASK DOCTOR

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

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

STOP USE

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

PURPOSE

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

WARNINGS

Warnings: For external use only.

DOSAGE & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

Neutracett

Aid 4-Healing

Skin Recovery Treatment

For Tattoo, tattoo removal

All natural / won’t stain

INGREDIENTS AND APPEARANCE

NEUTRACETT  TATTOO
allantoin glycerin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51435-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 mg  in 0.1 g
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYALURONIC ACID (UNII: S270N0TRQY)
PANTHENOL (UNII: WV9CM0O67Z)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
BENZOIC ACID (UNII: 8SKN0B0MIM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51435-002-01	28.3 g in 1 TUBE

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	Business Operations
COSMETIC ENTERPRISES LTD		017701475	manufacture