HELLO SUGAR- lidocaine hydrochloride cream 
Sambria Pharmaceuticals, LLC

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Drug Facts

Active ingredient

Lidocaine HCL 5.0% w/w

Purpose

Anorectal (Local Anesthetic)

Uses

For temporary relief of pain and discomfort

Warnings

For external use only.

Do not use on broken skin or if allergic to any ingredient.

When using this product use only as directed. Avoid contact with the eyes, rashes, or mucous membranes.

Stop use and ask doctor if condition worsens, or if symptoms persist for more than 7 days or return.

Keep out of reach of children and pets If swallowed get medical help or contact a Poison Control Center right away.

Directions

When Practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with tissue or a soft cloth before application.

Adults: Apply externally to the affected area.

Keep away from children under 12

Other information

Protect this product from excessive heat and direct sun.

Inactive ingredients

Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine

Product label

image description

HELLO SUGAR 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54723-031
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
EMU OIL (UNII: 344821WD61)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
LAURETH-7 (UNII: Z95S6G8201)  
TEA TREE OIL (UNII: VIF565UC2G)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: 56C14G5FWO)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54723-031-014 g in 1 PACKET; Type 0: Not a Combination Product07/10/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/10/2025
Labeler - Sambria Pharmaceuticals, LLC (078676259)

Revised: 7/2025
 
Sambria Pharmaceuticals, LLC