POST PEEL PROTECTANT VITALITY INSTITUTE- hydrocortisone cream

Post peel Protectant by

Drug Labeling and Warnings

Post peel Protectant by is a Otc medication manufactured, distributed, or labeled by Vi Medical Products Inc., VEGE-KURL, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients                   Purpose

Hydrocortisone 1% ................. Anti-itch

PURPOSE

Uses

• For the temporary relief of of itching associated with minor skin irritations and rashes due to
• Eczema
• insect bites
• poison ivy, poison oak, poison sumac
• soaps and detergents cosmetics
• jewelry

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center rigth away

INDICATIONS & USAGE

Stop use and ask a doctor

if condition worsens, or if symptoms persist for more than 7 day or clear up and occur again within a few days, do not use this or any other hydrocortisone products unless you hav consulted a doctor.

WARNINGS

Warnings

• For external use only
• Avoid Contact with eyes

DOSAGE & ADMINISTRATION

Directions

• Adults and children under 2 years of age and older: Appyl to affected area not more than 3 to 4 times daily
• Children under 2 years of age: Do not use, consult a doctor

INACTIVE INGREDIENT

Inactive Ingredients



Water (Aqua), Cyclopentasiloxane, Demthicone/Vinyl Dimethicone Crosspolymer, Aloe Barbadensis Leaf Juice, Glycerin, Cetearyl Alcohol, Ceteareth-20, Caprylic/Capric Triglyceride, Cetyl Alcohol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Avena Sativa (Oat) Kernel Extract, Chrysanthemum Pathenium (Feverfew) Extract, Tocophoneryl Acetate, Allantoint, Ethylhexylglycerin, Phenoxyethanol

PRINCIPAL DISPLAY PANEL

Vitality Institute

Skin Care System

Post Peel Protectant

Anti-itch Cream

30 mL/1 FL OZ

INGREDIENTS AND APPEARANCE

POST PEEL PROTECTANT  VITALITY INSTITUTE
hydrocortisone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70484-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	7.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETYL ALCOHOL (UNII: 936JST6JCN)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
OAT (UNII: Z6J799EAJK)
TANACETUM PARTHENIUM (UNII: 6GE7Z0761K)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALLANTOIN (UNII: 344S277G0Z)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70484-001-02	1 in 1 BOX	03/25/2015
1	NDC: 70484-001-01	30 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/25/2015

Labeler - Vi Medical Products Inc. (063910521)

Registrant - VEGE-KURL, INC (021072509)

Establishment
Name	Address	ID/FEI	Business Operations
VEGE-KURL, INC		021072509	manufacture(70484-001)