IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE TREATMENT- salicylic acid lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient


Salicylic acid 2%

Purpose

Acne treatment

Use

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

Inactive ingredients

water, glycerin, niacinamide, lactic acid, sodium hydroxide, zinc PCA, aloe barbadensis leaf juice, butylene glycol, chlorphenesin, sodium hyaluronate, trisodium ethylenediamine disuccinate, alteromonas ferment extract, citric acid, potassium sorbate, sodium benzoate

Questions or comments?

Call 800-620-3950

image of a carton

image of a carton
IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE TREATMENT 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-026
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
NIACINAMIDE (UNII: 25X51I8RD4)  
LACTIC ACID (UNII: 33X04XA5AT)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ZINC PIDOLATE (UNII: C32PQ86DH4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-026-011 in 1 CARTON04/01/2022
130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:49967-026-024 mL in 1 PACKET; Type 0: Not a Combination Product04/01/202204/01/2022
3NDC:49967-026-034 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00604/01/2022
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-026) , pack(49967-026)
Establishment
NameAddressID/FEIBusiness Operations
Dimensional Merchandising Inc.076693183pack(49967-026)

Revised: 12/2023
Document Id: 6ec7f0cb-c691-426f-afa2-dd8bb9814f5c
Set id: fd92c669-997e-4eea-b883-fe3486b83f31
Version: 2
Effective Time: 20231228
 
L'Oreal USA Products Inc