UP AND UP DUAL EFFECTS MOISTURIZER- salicylic acid lotion

Up and Up by

Drug Labeling and Warnings

Up and Up 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 Medication

INDICATIONS & USAGE

Uses

• For the management of acne.

Warnings

For external use only

WHEN USING

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. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions Cleanse 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 increase to two or three times daily if needed or as directed by doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

SPL UNCLASSIFIED SECTION

Other information may stain some fabrics

INACTIVE INGREDIENT

Inactive ingredients Water, Dicaprylyl Ether, Glycerin, Cetearyl Alcohol, Dimethicone, Neopentyl Glycol Diisostearate, Neopentyl Glycol Diethylhexanoate, Aluminum Starch Octenylsuccinate, Methyl Gluceth-20, Dicetyl Phosphate, Ceteth-10 Phosphate, Mentyl Lacatate, Steareth-21, Steareth-2, Fragrance, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Magnesium Aluminum Silicate, BHT.

PRINCIPAL DISPLAY PANEL

Up & Up Dual Effects Moisturizer

NET WT 4 OZ (118 mL)

NDC: 11673-931-53

INGREDIENTS AND APPEARANCE

UP AND UP  DUAL EFFECTS MOISTURIZER
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-931
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
STEARETH-2 (UNII: V56DFE46J5)
GLYCERIN (UNII: PDC6A3C0OX)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
WATER (UNII: 059QF0KO0R)
STEARETH-21 (UNII: 53J3F32P58)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
MENTHYL D-LACTATE, (-)- (UNII: XFS8QYW6WY)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
XANTHAN GUM (UNII: TTV12P4NEE)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-931-53	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/23/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/23/2019

Labeler - TARGET CORPORATION (006961700)

Registrant - Fruit Of The Earth, Inc. (079559467)

Establishment
Name	Address	ID/FEI	Business Operations
Fruit Of The Earth Research Laboratories, Inc.		008193513	manufacture(11673-931)