IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE TREATMENT- salicylic acid lotion

Pays: États-Unis

Langue: anglais

Source: NLM (National Library of Medicine)

Ingrédients actifs:

SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)

Disponible depuis:

L'Oreal USA Products Inc

Mode d'administration:

TOPICAL

Type d'ordonnance:

OTC DRUG

indications thérapeutiques:

Acne treatment - for the treatment of acne - helps prevent new acne blemishes from forming

Statut de autorisation:

OTC monograph final

Résumé des caractéristiques du produit

IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM ACNE
TREATMENT- SALICYLIC ACID LOTION
L'OREAL USA PRODUCTS INC
----------
DRUG FACTS
ACTIVE INGREDIENT
Salicylic acid 2%
PURPOSE
Acne treatment
USE
for the treatment of acne
helps prevent new acne blemishes from forming
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
clean the skin thoroughly before applying this product
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 ingrease to two or three times dialy if neded or as directed
by a doctor
if bothersome dryness or peeling occurs, reduce application to once a
day or every
other dayl
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
IT COSMETICS BYE BYE BREAKOUT CONCENTRATED DERMA SERUM
ACNE TREATMENT
salicylic acid lotion
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:49967-026
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)
SALICYLIC ACID
20 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
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 (