Label: BODY SCRUB- glycerin and kaolin gel
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Contains inactivated NDC Code(s)
NDC Code(s): 61671-003-01 - Packager: Milk & Co Pty Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 8, 2014
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
This Face + Body Scrub is the all over, multi tasking, timesaving type! It's been lightly scented with rosemary and peppermint, which helps gently exfoliate, cleanse, and moisturise your skin. It's made from marine ingredients which help enrich the skin, keeping it smooth, firm, and healthy. And finally we have added walnut shell, that's what you feel when scrubbing!
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Ingredients: water, polyethylene, cocamidopropyl betaine, sodium laureth sulphate, glycerin, juglans regia (walnut) shell powder, kaolin, carbomer, phenoxyethanol, hydroxyethylcellulose, tocopheryl acetate, spirulina maxima extract, propylene glycol, porphyra umbilicas (nori) extract, potassium hydroxide, panthenol, aloe barbadensis leaf juice, fragrance, disodium EDTA, methylchloroisothiazolinone, methylisothiazolinone.
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BODY SCRUB
glycerin and kaolin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61671-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 7.5 g in 375 g KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) KAOLIN 6 g in 375 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) EDETATE DISODIUM (UNII: 7FLD91C86K) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) JUGLANS REGIA SHELL (UNII: PJ10MT7VKA) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) PORPHYRA UMBILICALIS (UNII: 14AN0J70WO) WATER (UNII: 059QF0KO0R) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SPIRULINA MAXIMA (UNII: 9K7IG15M0Q) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61671-003-01 375 g in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/08/2014 Labeler - Milk & Co Pty Ltd (754955045) Establishment Name Address ID/FEI Business Operations Milk & Co Pty Ltd 754955045 manufacture(61671-003)
