AUEBLISS- lidocaine cream

Auebliss by

Drug Labeling and Warnings

Auebliss by is a Otc medication manufactured, distributed, or labeled by Jag Alliance, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine HCl 5%

Purpose

Topical analgesic/Anesthetic

Uses

For the temporary relief of minor pain, irritation and itching

Warnings

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

KEEP OUT OF REACH OF CHILDREN

Directions

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

Store at 15-30 C (59'-86' F).

Inactive ingredients

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 

855-700-0660

Product label

INGREDIENTS AND APPEARANCE

AUEBLISS 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73143-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73143-002-01	56 g in 1 TUBE; Type 0: Not a Combination Product	01/05/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/05/2023

Labeler - Jag Alliance, LLC (081456767)