HyVee Blemish Controlling Apricot Scrub

HyVee Blemish Controlling Apricot Scrub by

Drug Labeling and Warnings

HyVee Blemish Controlling Apricot Scrub by is a Otc medication manufactured, distributed, or labeled by HYVEE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HYVEE BLEMISH CONTROLLING APRICOT SCRUB- salicylic acid emulsion 
HYVEE INC

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HyVee Blemish Controlling Apricot Scrub

Active ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment

Uses

for the treatment of acne.

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

Keep out of reach of children.

If swallowed, get 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 fabric store at room temperature

Inactive ingredients

Water, Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Propylene Glycol, Sodium Laureth Sulfate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, PEG-100 Stearate, Glyceryl Stearate, Cetyl Acetate, Ceteareth-20, Polysorbate 60, Carbomer, Acetylated Lanolin Alcohol, Fragrance (Parfum), Phenethyl Alcohol, PPG-2-Methyl Ether, Limonene, Linalool, Methylisothiazolinone, Glycerin, Prunus Armeniaca (Apricot) Fruit Extract, Titanium Dioxide (CI177891).

HYVEE BLEMISH CONTROLLING APRICOT SCRUB 
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42507-930
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 g

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
CORN GRAIN (UNII: C1Z9U7094Z)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
APRICOT (UNII: 269CJD5GZ9)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ACETATE (UNII: 4Q43814HXS)
POLYSORBATE 60 (UNII: CAL22UVI4M)
TROLAMINE (UNII: 9O3K93S3TK)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42507-930-15	170 g in 1 TUBE; Type 0: Not a Combination Product	09/25/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/25/2013	03/17/2020

Labeler - HYVEE INC (006925671)

Revised: 10/2024

Document Id: 249b6f2d-b29e-799d-e063-6394a90a5ed0

34390-5

Set id: c69f8ec5-446e-153f-e053-2995a90a074d

Version: 2

Effective Time: 20241016