TARGET UP AND UP MOISTURIZER WITH SALICYLIC ACID ACNE TREATMENT- salicylic acid lotion

Target Up and Up Moisturizer with Salicylic Acid Acne Treatment by

Drug Labeling and Warnings

Target Up and Up Moisturizer with Salicylic Acid Acne Treatment by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne Treatment

Uses

for the treatment of acne

Warnings

For external use only.

When using this product

• skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one acne product at a time.
• avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children.

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

Directions

• cover the entire affected area with a thin layer and rinse thoroughly one to three times daily.
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
• 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.

Other Information

• may stain some fabrics

Inactive Ingredients

water, cetearyl alcohol, glycerin,
caprylic/capric triglyceride, dimethicone, cetearyl glucoside, arachidyl
alcohol, arachidyl glucoside, ceteareth-20, ceramide NP, ceramide AP,
ceramide EOP, phytosphingosine, sodium hyaluronate†, cholesterol,
ethylhexylglycerin, lecithin, polyglyceryl-3 diisostearate, niacinamide,
zinc PCA, potassium phosphate, dipotassium phosphate, sodium lauroyl
lactylate, behenyl alcohol, disodium EDTA, phenoxyethanol, caprylyl
glycol, hexylene glycol, carbomer, xanthan gum

Label

INGREDIENTS AND APPEARANCE

TARGET UP AND UP MOISTURIZER WITH SALICYLIC ACID ACNE TREATMENT 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ZINC PIDOLATE (UNII: C32PQ86DH4)
HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)
NIACINAMIDE (UNII: 25X51I8RD4)
DOCOSANOL (UNII: 9G1OE216XY)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
CERAMIDE AP (UNII: F1X8L2B00J)
WATER (UNII: 059QF0KO0R)
CHOLESTEROL (UNII: 97C5T2UQ7J)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
XANTHAN GUM (UNII: TTV12P4NEE)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
CERAMIDE NP (UNII: 4370DF050B)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-016-13	118 mL in 1 TUBE; Type 0: Not a Combination Product	09/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/30/2024

Labeler - TARGET CORPORATION (006961700)