Auebliss

Manufacturer: Jag Alliance, LLC
Effective date: 2023-01-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:52:58

Label at a glance#

ProductAuebliss

Active ingredientLIDOCAINE

Label structure9 sections

Indications and uses

For the temporary relief of minor pain, irritation and itching

Dosage and administration

Adults and children over 12 years: • Apply a thin layer to affected area every 6 to 8 hours. • Wash hands with soap and water immediately after use. • Children 12 years or younger: ask a doctor.

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact855-700-0660

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic/Anesthetic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor pain, irritation and itching

Warnings

WARNINGS SECTION

For external use only.
When using this product Avoid contact with eyes.
Do not apply to wounds or damaged, broken or irritated skin
Stop use and ask a doctor If• Condition worsens. • Irritation develops. Redness appears. • Symptoms persist for more than 7 days or clear up and occurs again within a few days.

Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away. Emergency Number: 1-800-222-1222

IF PREGNANT OR BREASTFEEDING, ask a heath professional before use

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:
• Apply a thin layer to affected area every 6 to 8 hours.
• Wash hands with soap and water immediately after use.
• Children 12 years or younger: ask a doctor.

Other Information

SPL UNCLASSIFIED SECTION

Store at 15•-30• C (59'-86' F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Caprylic/Capric Triglyceride, Butylene Glycol, Ethoxydiglycol, Ammonium AcryloyldimethyltaurateNP Copolymer, Squalane, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, Tocopherol (Vitamin E), Persea Gratissima (Avocado) Oil, Hydroxyethyl Acrylate, Sodium Acryloyldimethyl Tau rate Copolymer, Polyacrylate Crosspolymer-6, Phenoxyethanol, Xanthan Gum, Ethylhexylglycerin, Lecithin.

Questions and comments

SPL UNCLASSIFIED SECTION

855-700-0660

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LIDOCAINE 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
73143-002-01	2025-01-30	C162847	48780-1	2cef2736-87b4-d83d-e063-dadaa90ab31f	d7e394b6-3e88-445b-82eb-3b89d70eb8b3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73143-002-01	Auebliss	56 g in 1 TUBE	CREAM	56		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73143-002	AUEBLISS (LIDOCAINE) CREAM [JAG ALLIANCE, LLC]	1	Legacy NDC, 1 package rows	20230106_d7e394b6-3e88-445b-82eb-3b89d70eb8b3.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

Auebliss
Lidocaine
WATER
BUTYLENE GLYCOL
DIETHYLENE GLYCOL MONOETHYL ETHER
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
SQUALANE
ALOE VERA LEAF
ALLANTOIN
TOCOPHEROL
AVOCADO OIL
2-HYDROXYETHYL ACRYLATE
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)
PHENOXYETHANOL
XANTHAN GUM
ETHYLHEXYLGLYCERIN
LECITHIN, SOYBEAN
TRICAPRIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73143-002	73143-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
DIETHYLENE GLYCOL MONOETHYL ETHER	A1A1I8X02B	IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	W59H9296ZG	IACT
SQUALANE	GW89575KF9	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALLANTOIN	344S277G0Z	IACT
TOCOPHEROL	R0ZB2556P8	IACT
AVOCADO OIL	6VNO72PFC1	IACT
2-HYDROXYETHYL ACRYLATE	25GT92NY0C	IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%)	86FQE96TZ4	IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)	Q7UI015FF9	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
XANTHAN GUM	TTV12P4NEE	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
LECITHIN, SOYBEAN	1DI56QDM62	IACT
TRICAPRIN	O1PB8EU98M	IACT
LIDOCAINE	98PI200987	ACTIB

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
f183f9bf-558b-4a99-e053-2995a90a0878			d7e394b6-3e88-445b-82eb-3b89d70eb8b3	2023-01-05	Warnings	Exact identifier spl id: f183f9bf-558b-4a99-e053-2995a90a0878 spl set id: d7e394b6-3e88-445b-82eb-3b89d70eb8b3

Reported adverse events (FAERS/openFDA)#

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