BLEMISH CONTROL BASICS KIT- salicylic acid 
e.l.f. Cosmetics, Inc

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Blemish Control Basics Kit

Drug Facts

Active ingredients

Salicylic Acid 1%

Purpose

Acne Treatment

Uses

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.

Keep out of reach of children.

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

Directions

Cleanse the skin thoroughly before applying medication. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day. Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated eleswhere on this label.

Inactive ingredients

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Glycerin, Zinc PCA, Sodium Benzoate, Hydroxypropyl Methylcellulose, Sodium Hydroxide, Sodium Chloride, Citric Acid, Disodium EDTA, Niacinamide, Tranexamic Acid May Contain: Blue 1 (CI 42090), Yellow 5 (CI 19140)

Questions or comments

1-888-315-9814

Drug Facts

Active ingredients

Salicylic Acid 1%

Purpose

Acne Treatment

Uses

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.

Keep out of reach of children.

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

Directions

Cleanse the skin thoroughly before applying medication. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day. Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated eleswhere on this label.

Inactive ingredients

Water (Aqua), Niacinamide, Glycerin, Silica, Propanediol, Isododecane, Tranexamic Acid, Glyceryl Stearate Citrate, C12-15 Alkyl Benzoate, Acetyl Glucosamine, Tromethamine, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Cetearyl Alcohol, Capryloyl Glycine, Potassium Cetyl Phosphate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Xanthan Gum, Caprylyl Glycol, Ethylhexylglycerin, Tocopherol, Helianthus Annuus (Sunflowe) Seed Oil, Disodium EDTA, Caprylic Acid, Sodium Citrate May Contain: Chromium Oxide Greens (CI 77288), Iron Oxides (CI 77492)

Questions or comments

1-888-315-9814

Package Labeling: Kit

kit

Package Labeling: 30ml

label30

Package Labeling: 30ml

cream

BLEMISH CONTROL BASICS KIT 
salicylic acid kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-417
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-417-011 in 1 KIT02/25/2022
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 30 mL
Part 21 BOTTLE 30 mL
Part 1 of 2
ACNE CLARIFYING CLEANSER 
salicylic acid liquid
Product Information
Item Code (Source)NDC:76354-415
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
ZINC PIDOLATE (UNII: C32PQ86DH4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
NIACINAMIDE (UNII: 25X51I8RD4)  
TRANEXAMIC ACID (UNII: 6T84R30KC1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-415-021 in 1 CARTON
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00602/25/2022
Part 2 of 2
ACNE CALMING WATER CREAM 
salicylic acid cream
Product Information
Item Code (Source)NDC:76354-416
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
NIACINAMIDE (UNII: 25X51I8RD4)  
GLYCERIN (UNII: PDC6A3C0OX)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PROPANEDIOL (UNII: 5965N8W85T)  
ISODODECANE (UNII: A8289P68Y2)  
TRANEXAMIC ACID (UNII: 6T84R30KC1)  
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
N-ACETYLGLUCOSAMINE (UNII: V956696549)  
TROMETHAMINE (UNII: 023C2WHX2V)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
ALLANTOIN (UNII: 344S277G0Z)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
TOCOPHEROL (UNII: R0ZB2556P8)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
CAPRYLIC ACID (UNII: OBL58JN025)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-416-021 in 1 CARTON
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00602/25/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00602/25/2022
Labeler - e.l.f. Cosmetics, Inc (093902816)

Revised: 4/2024
Document Id: 16d7e219-bb4f-dfa1-e063-6394a90a1552
Set id: 1caf8dbb-18c2-48e9-a8b2-f4f53a4a32d2
Version: 4
Effective Time: 20240424
 
e.l.f. Cosmetics, Inc