ERASE IT KIT- salicylic acid, titanium dioxide, zinc oxide kit

ERASE IT KIT by

Drug Labeling and Warnings

ERASE IT KIT by is a Otc medication manufactured, distributed, or labeled by mybody. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT

SALICYLIC ACID 2%

PURPOSE

PURPOSE

ACNE TREATMENT

INDICATIONS & USAGE

USE FOR TREATMENT OF ACNE

WARNINGS

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

DO NOT USE * IF YOU HAVE VERY SENSITIVE SKIN OR ARE SENSITIVE TO SALICYLIC ACID.

ASK DOCTOR/PHARMACIST

ASK A DOCTOR OR PHARMACIST BEFORE USE IF *PREGNANT OR LACTATING. YOU ARE USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

WHEN USING

WHEN USING THIS PRODUCT * AVOID CONTACT WITH EYES. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. * KEEP AWAY FROM LIPS AND MOUTH.

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.

DOSAGE & ADMINISTRATION

DIRECTIONS

* USE AM/PM OR AS DIRECTED BY A DOCTOR. APPLY A NICKEL-SIZE AMOUNT TO WET HANDS. RUB TOGETHER. GENTLY MASSAGE ONTO FACE AND NECK WITH CIRCULAR MOTIONS. LEAVE ON 1-2 MINUTES THEN RINSE WELL.

OTHER SAFETY INFORMATION

OTHER INFORMATION

* AVOID STORAGE AT EXTREME TEMPERATURES (BELOW 40°F AND ABOVE 100°F).

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: WATER, DISODIUM LAURETH SULFOSUCCINATE, SODIUM COCOYL ISETHIONATE, SODIUM LAUROAMPHOACETATE, GLYCERIN, SODIUM METHYL COCOYL TAURATE, METHYLISOTHIAZOLINONE, COCAMIDOPROPYL BETAINE, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, OAT (AVENA SATIVA) KERNEL EXTRACT, DISODIUM EDTA, BETA GLUCAN, EUCALYPTUS GLOBULUS OIL, XANTHAN GUM, MENTHOL, MYRISTOYL TETRAPEPTIDE-13, ACETYL CARBOXYMETHYL COCOYL GLYCINE, PHENOXYETHANOL, CAPRYLYL GLYCOL.

QUESTIONS

QUESTIONS OR COMMENTS?

CALL 877.423.1314 * WWW.LOVEMYBODY.COM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ERASE IT KIT 
salicylic acid, titanium dioxide, zinc oxide kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49520-501

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49520-501-64	1 in 1 KIT

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1		1
Part 2		1
Part 3		1
Part 4		1

Part 1 of 4

PROTECT AND SERVE  TINTED SUN SHIELD SPF 30
titanium dioxide and zinc oxide lotion

Product Information
Item Code (Source)	NDC: 49520-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	11 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE (UNII: NMQ347994Z)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
CALCIUM BEHENATE (UNII: J5VFA9V6YG)
MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
ALUMINUM OXIDE (UNII: LMI26O6933)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
METHICONE (20 CST) (UNII: 6777U11MKT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
LYCOPENE (UNII: SB0N2N0WV6)
GLYCERIN (UNII: PDC6A3C0OX)
SUCROSE PALMITATE (UNII: 3OSQ643ZK5)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	09/23/2012

Part 2 of 4

TAKE CONTROL CALMING  CLEANSER
salicylic acid gel

Product Information
Item Code (Source)	NDC: 49520-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
GINGER (UNII: C5529G5JPQ)
OAT (UNII: Z6J799EAJK)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CURDLAN (UNII: 6930DL209R)
EUCALYPTUS OIL (UNII: 2R04ONI662)
XANTHAN GUM (UNII: TTV12P4NEE)
MENTHOL (UNII: L7T10EIP3A)
MYRISTOYL PENTAPEPTIDE-4 (UNII: PMA59A699X)
ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/27/2012

Part 3 of 4

LET ME CLARIFY 
salicylic acid gel

Product Information
Item Code (Source)	NDC: 49520-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
1,3-BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCOLIC ACID (UNII: 0WT12SX38S)
POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)
MYRISTOYL TETRAPEPTIDE-4 (UNII: 87AV1IB2EU)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/24/2012

Part 4 of 4

BREAK FREE 
lotions, oils, powders, and creams

Product Information
Item Code (Source)	NHRIC:49520-901

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
INGR	WATER (UNII: 059QF0KO0R)
INGR	PENTYLENE GLYCOL (UNII: 50C1307PZG)
INGR	COCO-GLYCERIDES (UNII: ISE9I7DNUG)
INGR	LAURYL LAURATE (UNII: GPW77G0937)
INGR	MYRISTOYL PENTAPEPTIDE-4 (UNII: PMA59A699X)
INGR	HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
INGR	4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)
INGR	SODIUM HYDROXIDE (UNII: 55X04QC32I)
INGR	EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
INGR	LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
INGR	POLYGLYCERIN-10 (UNII: P9060O936A)
INGR	CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
INGR	ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)
INGR	LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
INGR	TROMETHAMINE (UNII: 023C2WHX2V)
INGR	BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
INGR	CAPRYLYL GLYCOL (UNII: 00YIU5438U)
INGR	PHENOXYETHANOL (UNII: HIE492ZZ3T)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Cosmetic		09/24/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	05/10/2014

Labeler - mybody (004460532)