Blackhead Clearing Scrub

Blackhead Clearing Scrub

Drug Labeling and Warnings

Drug Details

k">

BLACKHEAD CLEARING SCRUB- salicylic acid gel 
Vi-Jon

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.

----------

Blackhead Clearing Scrub

Active ingredient

Salicylic acid (2%)

Purpose

Acne medication 

Uses 

  • for the treatment of acne
  • clears blackheads

Warnings

For external use only

When using this product

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.  If irritation occurs, only use one topical acne medication at a time.
  • avoid contact with the eyes.  If contact occurs, flush thoroughly with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

moisten face with water.  Apply product with wet fingertips and massage over face.  Rinse well and pat dry.

Other information

store at room temperature

Inactive ingredients

water, cetyl alcohol, PPG-15 stearyl ether, synthetic wax, microcrystalline wax, steareth-21, polysobate 60, potassium cetyl phosphate, xanthan gum, fragrance, menthyl lactate, jojoba esters, ferric ferrocyanide

*This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Clean & Clear Blackhead Clearing Scrub.

Manufactured by: Vi-Jon, Inc.,

St. Louis, MO 63114

Questions or comments? 1-888-593-0593

Made in the USA with US and foreign parts.

Principal display panel

Mountain Falls

*Compare to Clean & Clear

gently exfoliates

penetrates pres to eliminate most blackheads

polyethylene bead free

oil free

Blackhead Clearing Scrub

acne medication

NET WT 5 OZ (141 g)

image description

219.002/219AC

BLACKHEAD CLEARING SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0869-0219
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID19.4 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
STEARETH-21 (UNII: 53J3F32P58)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)  
FERRIC FERROCYANIDE (UNII: TLE294X33A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0869-0219-56141 g in 1 TUBE; Type 0: Not a Combination Product08/13/2007
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/13/2007
Labeler - Vi-Jon (790752542)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon790752542manufacture(0869-0219)
Establishment
NameAddressID/FEIBusiness Operations
Chemrite623776502manufacture(0869-0219)

Revised: 12/2018
 
Vi-Jon


© 2019 FDA.report
This site is not affiliated with or endorsed by the FDA.