FDA.reportPublic FDA data

Bare 40 Plus SA

Manufacturer
SSG Ventures Inc
Effective date
2021-02-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:10

Label at a glance#

ProductBare 40 Plus SA
Active ingredientUREA, SALICYLIC ACID
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

UREA 40%, SALICYLIC ACID 2%, TEA TREE OIL, ALOE VERA

OTC - PURPOSE SECTION

SOOTHES ROUGH & DRY SKIN

HEALS CORNS & CALLOUSES

INDICATIONS & USAGE SECTION

SOOTHES ROUGH & DRY SKIN

SAFE HANDLING WARNING SECTION

FOR EXTERNAL USE ONLY. AVOID CONTACT TO EYES.

KEEP OUT OF REACH OF CHILDREN. STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS.

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

INSTRUCTIONS FOR USE SECTION

APPLY TO AFFECTED AREA AT LEAST TWICE DAILY OR AS NEEDED.USE CONTINUOUSLY FOR 2-3 WEEKS FOR OPTIMAL RESULTS.

INACTIVE INGREDIENT SECTION

CARBOMER, XANTHAN GUM, MINERAL OIL, PROPYLENE GLYCOL,EMULSIFIERS, TRIETHANOLAMINE

STORAGE AND HANDLING SECTION

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

OTHER SAFETY INFORMATION

ENHANCED WITH TEA TREE OIL & ALOE VERA

DOSAGE & ADMINISTRATION SECTION

APPLY TO AFFECTED AREA AT LEAST TWICE DAILY OR AS NEEDED.USE CONTINUOUSLY FOR 2-3 WEEKS FOR OPTIMAL RESULTS.

WARNINGS SECTION

FOR EXTERNAL USE ONLY. AVOID CONTACT TO EYES. STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81376-222-012023-01-30C16284748780-1f386c64a-181e-0266-e053-dadaa90a7c1aBare 40 Plus SA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81376-222-01Bare 40 Plus SA113 g in 1 JARGEL1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81376-222BARE 40 PLUS SA (UREA) GEL [SSG VENTURES INC]1Legacy NDC, 1 package rows20210216_bb63f444-b729-56ee-e053-2a95a90a945e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81376-22281376-222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
XANTHAN GUMTTV12P4NEEIACT
MINERAL OILT5L8T28FGPIACT
COCONUT OILQ9L0O73W7LIACT
WATER059QF0KO0RIACT
TRIDECETH-10G624N6MSBAIACT
TEA TREE OILVIF565UC2GIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
UREA8W8T17847WACTIB
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

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
bb63f529-9059-7c02-e053-2a95a90a4961bb63f444-b729-56ee-e053-2a95a90a945e2021-02-15WarningsExact identifier
spl id: bb63f529-9059-7c02-e053-2a95a90a4961
spl set id: bb63f444-b729-56ee-e053-2a95a90a945e

Reported adverse events (FAERS/openFDA)#

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