Olivia Quido Skincare Blemish Eraser

Olivia Quido Skincare Blemish Eraser by

Drug Labeling and Warnings

Olivia Quido Skincare Blemish Eraser by is a Otc medication manufactured, distributed, or labeled by O Skin Care LLC, V Manufacturing & Logistics, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OLIVIA QUIDO SKINCARE BLEMISH ERASER- hydroquinone cream 
O Skin Care LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Olivia Quido Skincare Blemish Eraser

Drug Facts

Active Ingredient

Hydroquinone, 2%

Purpose

Skin Lightening

Uses

For the gradual fading of dark blemishes in the skin such as age spots, freckles, liver spots.

Warnings

For external use only.

Do Not Use on Children - under 12 years old of age unless directed by a physician.

Do not use on children - under 12 years of age unless directed by a physician.

Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor.

Keep out of eyes. Rinse water to remove.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults: apply a small amount as a thin layer on the affected area twice daily, or use as directed by a physician.
  • If no improvement is seen after 3 months of treatment, use of this product should be discontinued.
  • Lightening effect of this product may not be noticeable when used on dark skin.
  • Children under 12 years old: do not use unless directed by a physician.
  • Sun exposure should be limited by using a sunscreen agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

Other Information

  • Store at a controlled room temperature: 15°-30°C (59°-86°F), away from direct sunlight.

Inactive Ingredients

4-Butylresorcinol, Aloe Barbadensis Leaf Juice, BHT, C13-14 Isoparaffin, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oleosomes, Ceramide - NP, Cetyl Palmitate, Cetyl PEG/PPG-10/1 Dimethicone, Citric Acid, Diazolidinyl Urea, Dimethyl Isosorbide, Glycerin, Hexyl Laurate, Iodopropnyl Butylcarbamate, Kojic Acid, Laureth-23, Laureth-7, Maltodextrin, Phenoxyethanol, Polyacrylamide, Polyglyceryl-4 Isostearate, Polysorbate 20, Retinol, Silica, Sodium Hyaluronate, Sodium Hydroxide, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Trideceth-6 Phosphate, Triethylene Glycol, Water/Aqua.

OSCBE

OLIVIA QUIDO SKINCARE BLEMISH ERASER 
hydroquinone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 71421-501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
RETINOL (UNII: G2SH0XKK91)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
TRIDECETH-6 PHOSPHATE (UNII: NKT96BX1OC)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
4-BUTYLRESORCINOL (UNII: 2IK4UQ3ZGA)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)  
CERAMIDE NP (UNII: 4370DF050B)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
GLYCERIN (UNII: PDC6A3C0OX)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
KOJIC ACID (UNII: 6K23F1TT52)  
LAURETH-23 (UNII: N72LMW566G)  
LAURETH-7 (UNII: Z95S6G8201)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71421-501-301 in 1 CARTON07/27/202108/01/2024
130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/27/202108/01/2024
Labeler - O Skin Care LLC (021275401)
Registrant - V Manufacturing & Logistics, Inc. (825176857)
Establishment
NameAddressID/FEIBusiness Operations
V Manufacturing & Logistics, Inc.825176857manufacture(71421-501)

Revised: 8/2024
 

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