ULTRA REJUVE 7S AMPOULE

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 REJUVE 7S AMPOULE

Active ingredientGLYCERIN

Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: GLYCERIN 0.97%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: AQUA (WATER), PROPYLENE GLYCOL, PANTHENOL, PENTYLENE GLYCOL, PHENOXYETHANOL, HYDROLYZED WHEAT PROTEIN, CAPRYLYL/CAPRYL GLUCOSIDE, CENTELLA ASIATICA EXTRACT, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, PARFUM (FRAGRANCE), SACCHAROMYCES LYSATE, DISODIUM EDTA, TRITICUM VULGARE (WHEAT) SEED EXTRACT, ALGAE EXTRACT, SODIUM HYDROXIDE, o-CYMEN-5-OL, ETHYLHEXYLGLYCERIN, DISODIUM SUCCINATE, GLUTAMIC ACID, GLYCINE, THREONINE, VALINE, CITRIC ACID, POTASSIUM SORBATE, SODIUM BENZOATE, CI 19140 (FD&C YELLOW N°5)

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin rebalancing and nourishing

WARNINGS

WARNINGS SECTION

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

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

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Apply morning and night on clean face and neck prior to moisturizers

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71276-120-02	2020-01-31	C162847	48780-1	9d75b9d0-28ea-f424-e053-dadaa90a57ce	643f64bd-0b9d-43e5-95e4-0208a192c093

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71276-120-01	ULTRA REJUVE 7S AMPOULE	5 mL in 1 VIAL	LIQUID	5		1
71276-120-02	ULTRA REJUVE 7S AMPOULE	5 in 1 CARTON	LIQUID	5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71276-120	ULTRA REJUVE 7S AMPOULE (GLYCERIN) LIQUID [ULAB]	1	Legacy NDC, 2 package rows	20170322_643f64bd-0b9d-43e5-95e4-0208a192c093.zip

Products#

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

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

ULTRA REJUVE 7S AMPOULE
GLYCERIN
WATER
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71276-120	71276-120-01, 71276-120-02

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
GLYCERIN	PDC6A3C0OX	ACTIB
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	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
ba2089ba-60d7-4b38-8792-abcc76c65337			643f64bd-0b9d-43e5-95e4-0208a192c093	2017-03-22	Warnings	Exact identifier spl id: ba2089ba-60d7-4b38-8792-abcc76c65337 spl set id: 643f64bd-0b9d-43e5-95e4-0208a192c093

Reported adverse events (FAERS/openFDA)#

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