FDA.reportPublic FDA data

SUPER SPOT REMOVER ACNE TREATMENT

Manufacturer
ORIGINS NATURAL RESOURCES INC. | Estee Lauder Companies Inc. | The Estee Lauder Inc
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
15
Source
full-release
Hydrated at
2026-06-01 01:25:28

Label at a glance#

ProductSUPER SPOT REMOVER ACNE TREATMENT
Active ingredientSALICYLIC ACID
Label structure7 sections

Indications and uses

for the management of acne clears acne blemishes helps prevent development of new acne blemishes

Dosage and administration

Cleanse skin thoroughly before applying 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 a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

  • for the management of acne
  • clears acne blemishes
  • helps prevent development of new acne blemishes

Warnings

WARNINGS SECTION

For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, call a doctor or contact a Poison Control Center right away.

When using this product

OTC - WHEN USING SECTION

skin irritation and dryness is more likely to occur if you use another topical medication at the same time. If this occurs, only use one toptical acne medication at the same time. If this occurs, only use one topical acne medication at a time.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Cleanse skin thoroughly before applying
  • 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 a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol denat.,hamamelis virginiana (witch hazel) water,water\aqua\eau,acrylates/c10-30 alkyl acrylate crosspolymer,cucumis sativus (cucumber) fruit extract,pyrus malus (apple) fruit extract,scutellaria baicalensis root extract,algae extract,poria cocos sclerotium extract,laminaria saccharina extract,lactobacillus ferment,glycerin,caffeine,butylene glycol,tocopheryl acetate,magnesium ascorbyl phosphate,sodium hydroxide,eugenia caryophyllus (clove) bud oil1,origanum heracleoticum flower oil1,eugenol,sodium sulfite,sodium metabisulfite,disodium edta,phenoxyethanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORIGINS

Super Spot
Remover ™

Acne treatment gel

salicylic acid 1.5%

.3 fl. oz./oz. liq./10 ml e

CARTONCARTON

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416212salicylic acid 1.5 % Topical GelPSN15
2468334Super Spot Remover 1.5 % Topical GelPSN15
2468334salicylic acid 0.015 MG/MG Topical Gel [Super Spot Remover]SBD15
416212salicylic acid 0.015 MG/MG Topical GelSCD15
416212salicylic acid 1.5 % Topical GelSY15
2468334Super Spot Remover 0.015 MG/MG Topical GelSY15
2468334Super Spot Remover 1.5 % Topical GelSY15

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128012164AW 0J3M01111L 99770.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59427-005-012020-12-10C16284748780-19d75b9d0-5b60-f424-e053-dadaa90a57ceSUPER SPOT REMOVER™ ACNE TREATMENT
59427-005-012020-01-31C16284748780-19d75b9d0-5b60-f424-e053-dadaa90a57ceSUPER SPOT REMOVER™ ACNE TREATMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59427-005-01SUPER SPOT REMOVER ACNE TREATMENT1 in 1 CARTONGEL115
59427-005-01SUPER SPOT REMOVER ACNE TREATMENT10 mL in 1 CONTAINERGEL1015

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
.alpha.-tocopherol acetateINACTIVE INGREDIENT9E8X80D2L01
appleINACTIVE INGREDIENTB423VGH5S91
butylene glycolINACTIVE INGREDIENT3XUS85K0RA1
caffeineINACTIVE INGREDIENT3G6A5W338E1
clove oilINACTIVE INGREDIENT578389D6D01
cucumberINACTIVE INGREDIENTYY7C30VXJT1
eugenolINACTIVE INGREDIENT3T8H1794QW1
glycerinINACTIVE INGREDIENTPDC6A3C0OX1
magnesium ascorbyl phosphateINACTIVE INGREDIENT0R822556M51
phenoxyethanolINACTIVE INGREDIENTHIE492ZZ3T1
saccharina latissimaINACTIVE INGREDIENT68CMP2MB551
scutellaria baicalensis rootINACTIVE INGREDIENT7J95K7ID2S1
sodium hydroxideINACTIVE INGREDIENT55X04QC32I1
waterINACTIVE INGREDIENT059QF0KO0R1
witch hazelINACTIVE INGREDIENT101I4J0U341

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59427-00559427-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM SULFITEVTK01UQK3GIACT
SODIUM METABISULFITE4VON5FNS3CIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT
ORIGANUM VULGARE SUBSP. HIRTUM FLOWER3799SP11NYIACT
WATER059QF0KO0RIACT
CLOVE OIL578389D6D0IACT
EUGENOL3T8H1794QWIACT
CUCUMBERYY7C30VXJTIACT
APPLEB423VGH5S9IACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
SACCHARINA LATISSIMA68CMP2MB55IACT
GLYCERINPDC6A3C0OXIACT
CAFFEINE3G6A5W338EIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MAGNESIUM ASCORBYL PHOSPHATE0R822556M5IACT
SODIUM HYDROXIDE55X04QC32IIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FU LINGXH37TWY5O4IACT
LIMOSILACTOBACILLUS FERMENTUM2C1F12C6APIACT
PORPHYRIDIUM PURPUREUMK2P8K2558NIACT
ALCOHOL3K9958V90MIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 26 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
sodium hydroxideSODIUM HYDROXIDE55X04QC32IGEL / TOPICAL70 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
butylene glycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii+route
2 equally ranked IID candidates
glycerinGLYCERINPDC6A3C0OXGEL / TOPICAL500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338EGRANULE / ORALNAExact identifier — unii candidate
6 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
6 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338ESOLUTION / OPHTHALMIC2 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338EGRANULE / ORALNAExact identifier — unii candidate
6 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
6 equally ranked IID candidates
phenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
6 equally ranked IID candidates
sodium hydroxideSODIUM HYDROXIDE55X04QC32IGEL / TOPICAL70 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338ESPRAY, METERED / NASAL10 mg/1mlExact identifier — unii candidate
6 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
6 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
6 equally ranked IID candidates
butylene glycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii+route
2 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338ESOLUTION / OPHTHALMIC2 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
glycerinGLYCERINPDC6A3C0OXGEL / TOPICAL500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
caffeineCAFFEINE3G6A5W338ESPRAY, METERED / NASAL10 mg/1mlExact identifier — unii candidate
6 equally ranked IID candidates
phenoxyethanolPHENOXYETHANOLHIE492ZZ3TGEL / TOPICAL14 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
6 equally ranked IID candidates
clove oilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
6 equally ranked IID candidates
.alpha.-tocopherol acetate.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
6 equally ranked IID candidates

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
SUPER SPOT REMOVER ACNE TREATMENTSALICYLIC ACIDORIGINS NATURAL RESOURCES INC.a0aece76-008b-4af3-be39-13156acc73af2025-12-15WarningsExact identifier
ndc (package): 59427-005-01
ndc (product): 59427-005
ndc11 (package): 59427000501
spl id: 46011cef-0255-9f06-e063-6394a90ad2f4
spl set id: a0aece76-008b-4af3-be39-13156acc73af

Reported adverse events (FAERS/openFDA)#

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