Label: NO ZIT SHERLOCK ACNE CORRECTING- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 67038-106-30, 67038-106-31 - Packager: Bliss World LLC
- 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 June 4, 2012
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients
- Purposes
- Keep Out of Reach of Children
- Uses
- Warnings
- Directions
- Other information
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Inactive Ingredients
Inactive Ingredients
water, alcohol denat., butylene glycol, hamamelis virginiana (witch hazel) water, polysorbate 20, ethoxydiglycol, xanthan gum, hydroxyethylcellulose, sodium hydroxide, algae extract, yogurt extract, glucosamine HCL, fragrance, hamamelis virginiana (witch hazel) extract, saccharomyces cerevisiae extract, tetrahexyldecyl ascorbate, urea, aloe barbadensis leaf juice, spiraea ulmaria extract
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Package Label
bliss from our spa to your skin PROBIOTIC POWERED
no 'zit' sherlock acne system correcting serumhelps fade post-pimple pigmentation minimizes the appearance of large pores evens skin's tone and texture
why we're 'pro' probiotics Probiotics (like the yogurt and meadowsweet extract found in this moisturizer) are 'beneficial' bacteria similar to those found in your own body. They help boost skin's natural defenses against bacteria and create a healthier environment.
bliss dist Bliss New York NY 10013 USA London HA3 6DO UK 1003-02250 Made in USA blissworld.com
30mL/1 fl oz 1001-02252-208 -
INGREDIENTS AND APPEARANCE
NO ZIT SHERLOCK ACNE CORRECTING
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67038-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) POLYSORBATE 20 (UNII: 7T1F30V5YH) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) UREA (UNII: 8W8T17847W) ALOE VERA LEAF (UNII: ZY81Z83H0X) FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67038-106-30 15 mL in 1 TUBE 2 NDC:67038-106-31 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 04/01/2010 Labeler - Bliss World LLC (077427396) Registrant - Bliss World LLC (077427396)