ULTRA REPAIR

Manufacturer: ULAB | U-LAB Switzerland AG
Effective date: 2017-03-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:49:20

Label at a glance#

ProductULTRA REPAIR

Active ingredientSHEA BUTTER

Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: SHEA BUTTER 4.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aqua (WATER), CAPRYLIC/CAPRIC TRIGLYCERIDE, ISOHEXADECANE, PEG-8 BEESWAX, MARIS AQUA (SEA WATER), MACADAMIA INTEGRIFOLIA SEED OIL, CETYL ALCOHOL, POLYACRYLAMIDE, PROPYLENE GLYCOL DIPELARGONATE, PHENOXYETHANOL, GLYCERYL STEARATE, PROPANEDIOL, C13-14 ISOPARAFFIN, HYDROXYACETOPHENONE, THEOBROMA GRANDIFLORUM SEED BUTTER, PROPYLENE GLYCOL, CETETH-20, TOCOPHERYL ACETATE, STEARETH-20, CENTELLA ASIATICA EXTRACT, LAURETH-7, GLYCERIN, PARFUM (FRAGRANCE), TOCOPHEROL, NYMPHAEA ALBA FLOWER EXTRACT, POTASSIUM SORBATE, CITRIC ACID, TROPOLONE, GARDENIA TAHITENSIS FLOWER EXTRACT, CUCURBITA PEPO (PUMPKIN) SEED EXTRACT, SODIUM HYDROXIDE, SODIUM BENZOATE

PURPOSE

OTC - PURPOSE SECTION

Purpose: Moisturizing and soothing sensitized skin

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: Apply morning and night

WARNINGS

WARNINGS SECTION

Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Apply morning and night to face and neck after serum and ampoule

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71276-090-02	2020-01-31	C162847	48780-1	9d75b9d0-8260-f424-e053-dadaa90a57ce	c21e1f4c-e670-4dd1-a681-2337d8383767

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71276-090-01	ULTRA REPAIR	60 mL in 1 BOTTLE, PUMP	CREAM	60		1
71276-090-02	ULTRA REPAIR	1 in 1 CARTON	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71276-090	ULTRA REPAIR (SHEA BUTTER) CREAM [ULAB]	1	Legacy NDC, 2 package rows	20170322_c21e1f4c-e670-4dd1-a681-2337d8383767.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

ULTRA REPAIR
SHEA BUTTER
WATER
ISOHEXADECANE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71276-090	71276-090-01, 71276-090-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SHEA BUTTER	K49155WL9Y	ACTIB
WATER	059QF0KO0R	IACT
ISOHEXADECANE	918X1OUF1E	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
08a33e6f-915f-4f1c-8cfc-91cba2d1352d			c21e1f4c-e670-4dd1-a681-2337d8383767	2017-03-22	Warnings	Exact identifier spl id: 08a33e6f-915f-4f1c-8cfc-91cba2d1352d spl set id: c21e1f4c-e670-4dd1-a681-2337d8383767

Reported adverse events (FAERS/openFDA)#

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