FDA.reportPublic FDA data

Medicated Apricot Scrub

Manufacturer
United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC
Effective date
2026-02-16
Label type
HUMAN OTC DRUG LABEL
Version
17
Source
full-release
Hydrated at
2026-06-01 01:46:08

Label at a glance#

ProductMedicated Apricot Scrub
Active ingredientSALICYLIC ACID
Label structure13 sections

Dosage and administration

moisten face with water. Apply product with wet fingertips and masage over face. Rinse well and pat dry. avoid contact with the eyes. If contact occurs, flush thoroughly with water.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%

Purpose

OTC - PURPOSE SECTION

Acne medication

Use

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is more likely to occure 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • moisten face with water. Apply product with wet fingertips and masage over face. Rinse well and pat dry.
  • avoid contact with the eyes. If contact occurs, flush thoroughly with water.

Other information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, Juglans regia (walnut) shell powder, glyceryl stearate SE, glycerin, cetearyl alcohol, cetyl alcohol, decyl glucoside, cellulose, sodium hydroxide, cocamidopropyl betaine, glyceryl stearate, PEG-100 stearate, Prunus armeniaca (apricot) fruit extract, ceteareth-20, carbomer, polysorbate 60, fragrance, hydroxyacetophenone, phenoxyethanol, benzyl alcohol, limonene, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

Call 1-855-423-2630

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by ELIDA BEAUTY US (IP) LLC, distributor of St. Ives ® Acne Control Apricot Face Scrub.

Adverse reaction

ADVERSE REACTIONS SECTION

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

PROVIDENCE, RI 02908 USA

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQUALINE ®

COMPARE TO St. Ives ®Acne Control Apricot Face Scrub*

BLEMISH AND BLACKHEAD CONTROL

Medicated Apricot Scrub

salicylic acid acne medication with a natural exfoliant

dermatologist tested

exfoliates to prevent blemishes and cleanse pores

NET WT 6 0Z (170 g)

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN17
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD17
562600salicylic acid 2 % Facial Cleanser TonerSY17
562600salicylic acid 2 % Facial ScrubSY17
562600salicylic acid 2 % Medicated Liquid SoapSY17

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0014163TGmm01.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41163-041-302021-10-07C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.006/041AK Medicated Apricot Scrub
41163-041-302021-10-07C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.008/041AM Medicated Apricot Scrub
41163-041-302021-10-07C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.008/041AM Medicated Apricot Scrub
41163-041-302021-07-23C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.006/041AK Medicated Apricot Scrub
41163-041-302021-07-23C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.008/041AM Medicated Apricot Scrub
41163-041-302021-07-23C16284748780-1c7ccaba7-1d6a-fd44-e053-dadaa90aa01bEqualine 041.008/041AM Medicated Apricot Scrub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-041-30Medicated Apricot Scrub170 g in 1 TUBEGEL17017

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41163-04141163-041-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
JUGLANS REGIA SHELLPJ10MT7VKAIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
GLYCERINPDC6A3C0OXIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETYL ALCOHOL936JST6JCNIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
POWDERED CELLULOSESMD1X3XO9MIACT
SODIUM HYDROXIDE55X04QC32IIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
APRICOT269CJD5GZ9IACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
POLYSORBATE 60CAL22UVI4MIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZYL ALCOHOLLKG8494WBHIACT
LIMONENE, (+)-GFD7C86Q1WIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
162025-09-03monthly-update2026-06-03 17:38:41
152024-03-08full-release2026-06-01 00:09:38

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Medicated Apricot ScrubSALICYLIC ACIDUnited Natural Foods, Inc. dba UNFI677c19eb-780b-479b-ab1d-df249e0af6ea2026-02-16Warnings, Adverse reactionsExact identifier
ndc (package): 41163-041-30
ndc (product): 41163-041
ndc11 (package): 41163004130
spl id: 4af6bd00-f6d4-b7ee-e063-6394a90a591e
spl set id: 677c19eb-780b-479b-ab1d-df249e0af6ea

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.