BARE 40 urea gel

Manufacturer: Scientific Solutions Global, LLC
Effective date: 2018-03-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:54:58

Label at a glance#

ProductBare 40

Active ingredientUREA

Label structure10 sections

Dosage and administration

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

Storage and handling

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

UREA

OTC - PURPOSE SECTION

HEALS CORNS & CALLUSES

INDICATIONS & USAGE SECTION

SOOTHES ROUGH & DRY SKIN

SOFTEN NAILS

MOISTURIZING GEL

SAFETY WARNING :

WARNINGS SECTION

FOR EXTERNAL USE ONLY. AVOID CONTACT TO EYES.

STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

APPLY TO AFFECTED AREA AT LEAST TWICE DAILY OR AS NEEDED.

USE CONTINUOUSLY FOR 2-3 WEEKS FOR OPTIMAL RESULTS.

INACTIVE INGREDIENTS :

INACTIVE INGREDIENT SECTION

TEA TREE OIL, ALOE VERA, CARBOMER, XANTHAN GUM, MINERAL OIL, PROPYLENE GLYCOL,TRIETHANOLAMINE, EMULSIFIERS, COCONUT OIL, PRESERVED WATER

STORAGE AND HANDLING SECTION

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

SPL UNCLASSIFIED SECTION

ENHANCED WITH ALOE VERA & TEA TREE OIL

MAXIMUM STRENGTH

VISIT US AT : UREAEVERYTHING.COM

PACKAGING:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BARE40 UREA GEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
349352	urea 40 % Topical Gel	PSN	2
349352	urea 0.4 MG/MG Topical Gel	SCD	2
349352	urea 40 % Topical Gel	SY	2

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0612520315160	GTIN-13: 0612520315160 EAN-13: 0612520315160 GTIN-12: 612520315160 UPC-A: 612520315160 GTIN storage (14 digits): 00612520315160	Label-1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71718-002-01	2020-01-31	C162847	48780-1	9d75b9d0-69df-f424-e053-dadaa90a57ce	BARE 40 urea gel
71718-002-02	2020-01-31	C162847	48780-1	9d75b9d0-69df-f424-e053-dadaa90a57ce	BARE 40 urea gel
71718-002-03	2020-01-31	C162847	48780-1	9d75b9d0-69df-f424-e053-dadaa90a57ce	BARE 40 urea gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71718-002-01	Bare 40	113 g in 1 JAR	GEL	113	2
71718-002-02	Bare 40	113 g in 1 JAR	GEL	113	2
71718-002-02	Bare 40	2 in 1 PACKAGE	GEL	2	2
71718-002-03	Bare 40	226 g in 1 TUBE	GEL	226	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71718-002	BARE 40 (UREA) GEL [SCIENTIFIC SOLUTIONS GLOBAL, LLC]	2	Legacy NDC, 4 package rows	20180322_9c1199ae-c932-4291-b512-c263b9b8f968.zip

Products#

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

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

Bare 40
UREA
TEA TREE OIL
ALOE VERA LEAF
CARBOXYPOLYMETHYLENE
XANTHAN GUM
MINERAL OIL
PROPYLENE GLYCOL
TROLAMINE
COCONUT OIL
WATER
TRIDECETH-10

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71718-002	71718-002-01, 71718-002-02, 71718-002-03

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
Name	UNII	Kind
UREA	8W8T17847W	ACTIB
TEA TREE OIL	VIF565UC2G	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOXYPOLYMETHYLENE	0A5MM307FC	IACT
XANTHAN GUM	TTV12P4NEE	IACT
MINERAL OIL	T5L8T28FGP	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TROLAMINE	9O3K93S3TK	IACT
COCONUT OIL	Q9L0O73W7L	IACT
WATER	059QF0KO0R	IACT
TRIDECETH-10	G624N6MSBA	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a66b9eda-7266-4c8f-839e-4de0499ac960			9c1199ae-c932-4291-b512-c263b9b8f968	2018-03-22	Warnings	Exact identifier spl id: a66b9eda-7266-4c8f-839e-4de0499ac960 spl set id: 9c1199ae-c932-4291-b512-c263b9b8f968

Reported adverse events (FAERS/openFDA)#

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