BUNNIES BUM ANORECTAL NUMBING- lidocaine spray

Bunnies Bum Anorectal Numbing by

Drug Labeling and Warnings

Bunnies Bum Anorectal Numbing by is a Otc medication manufactured, distributed, or labeled by FloCal Distributors LLC, Derma Care Research Labs LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 5%

PURPOSE

Topical anesthetic

INDICATIONS & USAGE

Helps relieve the local itching and pain associated with anorectal disorders or inflammation.

WARNINGS

For external use only.

Flammable. Keep away from excessive heat or open flame.

When using this product

• avoid contact with eyes
• do not exceed recommended dosage unless directed by a doctor
• do not put this into the rectum by using fingers or any mechanical device or applicator
• contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F.

Stop use and ask a doctor if

• rectal bleeding occurs
• condition worsens or does not improve within 7 days
• allergic reaction occurs to ingredients in this product
• symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase

PREGNANCY OR BREAST FEEDING

Ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

• When practical, cleanse the affected area with mild soap and warm water, rinse thoroughly and gently pat dry. Spray affected area, wash hands after applying.
• Adults and children 12 years and older: apply externally to the affected area up to 6 times a day
• Children under 12 years of age: consult a doctor.

INACTIVE INGREDIENT

Alcohol denat., aloe barbadensis leaf extract, carbomer, chamomilla recutita (matricaria) flower extract, cucumis sativus (cucumber) fruit extract, disodium cocoamphodipropionate, disodium EDTA, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BUNNIES BUM ANORECTAL NUMBING 
lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84308-173
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
ALCOHOL (UNII: 3K9958V90M)
CARBOMER 940 (UNII: 4Q93RCW27E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CHAMOMILE (UNII: FGL3685T2X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CUCUMBER (UNII: YY7C30VXJT)
DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84308-173-05	142 g in 1 CAN; Type 0: Not a Combination Product	06/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	06/02/2025

Labeler - FloCal Distributors LLC (128775688)

Registrant - Derma Care Research Labs LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs LLC		116817470	manufacture(84308-173)