NDC 60949-010 By Pharmicell Lab The Prestige

NDC Product Code 60949-010

NDC 60949-010-01

Package Description: 50 g in 1 CARTON

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

By Pharmicell Lab The Prestige with NDC 60949-010 is a product labeled by Pharmicell Co., Ltd.. The generic name of By Pharmicell Lab The Prestige is . The product's dosage form is and is administered via form.

Labeler Name: Pharmicell Co., Ltd.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pharmicell Co., Ltd.
Labeler Code: 60949
Start Marketing Date: 10-01-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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By Pharmicell Lab The Prestige Product Label Images

By Pharmicell Lab The Prestige Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Active ingredient : GLYCERIN 20%

Inactive Ingredient

Inactive ingredients : WATER, HUMAN BONE MARROW STEM CELL CONDITIONED MEDIA, BUTYLENE GLYCOL, CETYL ETHYLHEXANOATE, HYDROGENATED POLYDECENE, CETEARYL ALCOHOL, NIACINAMIDE, HYDROGENATED VEGETABLE OIL, VEGETABLE OIL, BUTYROSPERMUM PARKII(SHEA BUTTER), DIPENTAERYTHRITYL HEXA C5-9 ACID ESTERS, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, CITRUS PARADISI (GRAPEFRUIT) FRUIT EXTRACT, STEARIC ACID, CETEARETH-20, DIMETHICONE, GLYCERYL STEARATE, MACADAMIA TERNIFOLIA SEED OIL, CETYL PEG/PPG-10/1 DIMETHICONE, 1,2-HEXANEDIOL, PHENOXYETHANOL, HYDROGENATED LECITHIN, XANTHAN GUM, SODIUM POLYACRYLATE, PANAX GINSENG ROOT EXTRACT, CLADOSIPHON OKAMURANUS EXTRACT, ALTHAEA ROSEA ROOT EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, CERAMIDE 3, NEOFINETIA FALCATA CALLUS CULTURE EXTRACT, ZANTHOXYLUM PIPERITUM FRUIT EXTRACT, PULSATILLA KOREANA EXTRACT, USNEA BARBATA (LICHEN) EXTRACT, LECITHIN, DEXTRIN, POLYACRYLATE-13, POLYISOBUTENE, POLYSORBATE 20, ADENOSINE, CITRUS MEDICA LIMONUM (LEMON) FRUIT OIL, JASMINUM OFFICINALE (JASMINE) OIL, ROSA CENTIFOLIA FLOWER OIL, SODIUM HYALURONATE

Purpose

Purpose : Skin Protectant

Warnings

Warning : Keep out of reach of children and babies. For external use only. Avoid contact with eyes. Discontinue use if signs of irritation and/or rash appear.

Keep Out Of Reach Of Children

Keep out of reach of children and babies.

Indications And Usage

Indications and usage : After taking the cream with a size of pea using a spatula, spread it evenly over the face and neck, and massage gently with both hands

Dosage And Administration

Dosage and administration : Take a proper amount of the product and spread it evenly over the entire face.

* Please review the disclaimer below.