MEDITOWEL ILLUMINATING SKIN BRIGHTENING- hydroquinone cloth

MEDITOWEL by

Drug Labeling and Warnings

MEDITOWEL by is a Otc medication manufactured, distributed, or labeled by MICRO CONNECTION ENTERPRISES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT (IN EACH WIPE)

HYDROQUINONE 2%

PURPOSE

SKIN LIGHTENER

USES

• WORKS DEEP IN THE SKIN'S SURFACE TO FADE SPOTS OVER TIME.

WARNINGS

FOR EXTERNAL USE ONLY

STOP AND ASK A DOCTOR IF SKIN IRRITATION BECOMES SEVERE.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY. POISON CONTROL CENTER # 1-800-222-1222.

DIRECTIONS

• UNFOLD TOWELETTE COMPLETELY, APPLY TO CLEAN DRY SKIN.
• KEEP AWAY FROM EYES, LIPS AND MOUTH.
• AVOID PRODUCT CONTACT WITH HAIR AND DYED FABRICS, INCLUDING CARPETS AND CLOTHING WHICH MAY BE BLEACHED BY THIS PRODUCT.
• LIGHTENING EFFECT OF THIS PRODUCT MAY NOT BE NOTICEABLE WHEN USED ON VERY DARK SKIN.
• THIS PRODUCT MAY DARKEN OVER TIME WHICH IS NORMAL AND DOES NOT AFFECT THE PRODUCT PERFORMANCE.
• FOR FASTER RESULTS, EXFOLIATE 2 TO 3 TIMES A WEEK.
• DISCARD AFTER USE

INACTIVE INGREDIENTS

PROPYLENE GLYCOL, GLYCERIN, WATER, ALOE VERA GEL, ARNICA EXTRACT, SODIUM METABISULFATE, ALLANTOIN, BISABOLOL, METHYLPARABEN, PROPYLPARABEN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDITOWEL  ILLUMINATING SKIN BRIGHTENING
hydroquinone cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76038-090
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
ALOE (UNII: V5VD430YW9)
ARNICA CHAMISSONIS FLOWER (UNII: 88WK5I8R3L)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76038-090-21	25 in 1 BOX	01/01/2011
1	NDC: 76038-090-01	1 mL in 1 POUCH; 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	part358A	01/01/2011

Labeler - MICRO CONNECTION ENTERPRISES INC (144297160)

Registrant - MICRO CONNECTION ENTERPRISES INC (144297160)

Establishment
Name	Address	ID/FEI	Business Operations
MICRO CONNECTION ENTERPRISES INC		144297160	manufacture(76038-090)