GEMBOOXT TOPICAL NUMBING CREAM- lidocaine hcl cream

Gembooxt Topical Numbing Cream by

Drug Labeling and Warnings

Gembooxt Topical Numbing Cream by is a Otc medication manufactured, distributed, or labeled by Guangdong Quadrant Ecological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

LIDOCAINE HCL 5%

PURPOSE

Local Anesthetic

INDICATIONS & USAGE

For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders.
For the temporary relief of pain,bumning and soreness

WARNINGS

For external use only

DO NOT USE

Do not use on broken or irritated skin.

WHEN USING

When using this product:
Use only as much as recommended,unless a doctor advises otherwise.
Do not insert into the rectum with fingers or any mechanical device or applicator.

STOP USE

Stop use and ask a doctor if
An allergic reaction is observed Symptoms such as redness, irritation,swelling, pain, orothers begin or worsen.
Does not show improvement within 7 days If pregnant or breast-feeding, ask a doctor before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed get medical help or contact a Poison Gontrol Center right away

DOSAGE & ADMINISTRATION

For adults and children 12 years and older:
When practical, clean the area with mild soap and warm water and rinse thoroughly Gently dry by patting or blotting with toilet tissue or a soft cloth before applying.
Apply up to 6 times daily.
Children under 12 years. Ask a doctor.

INACTIVE INGREDIENT

WATER
CETYL ALCOHOL
STEARYL ALCOHOL
GLYCERIN
MINERAL OIL
SODIUM POLYACRYLOYLDIMETHYL TAURATE
HYDROGENATED POLYDECENE
TRIDECETH-10
CETEARETH-25
STEARIC ACID
GLYCERYL STEARATE
DIMETHICONE
BENZYL ALCOHOL
PHENOXYETHANOL
BENZOIC ACID
ARNICA MONTANA FLOWER EXTRACT
TRIETHANOLAMINE
EUCALYPTUS GLOBULUS LEAF OIL
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
XANTHAN GUM
POTASSIUM LAURYL PHOSPHATE
DIPOTASSIUM PHOSPHATE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GEMBOOXT TOPICAL NUMBING CREAM 
lidocaine hcl cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76986-023
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HCL (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	0.05 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TRIDECETH-10 (UNII: G624N6MSBA)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: NG5NG5733T)
POTASSIUM LAURYL PHOSPHATE (UNII: C4QT53N4MK)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETEARETH-25 (UNII: 8FA93U5T67)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
BENZOIC ACID (UNII: 8SKN0B0MIM)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
EUCALYPTUS GLOBULUS OIL (UNII: 2R04ONI662)
CETYL ALCOHOL (UNII: 936JST6JCN)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76986-023-01	50 g in 1 BOTTLE; Type 0: Not a Combination Product	01/30/2026
2	NDC: 76986-023-02	60 g in 1 BOTTLE; Type 0: Not a Combination Product	01/30/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/30/2026

Labeler - Guangdong Quadrant Ecological Technology Co., Ltd. (554532634)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Quadrant Ecological Technology Co., Ltd.		554532634	manufacture(76986-023)