WILL RELIEVE ROLL-ON- lidocaine hydrochloride gel

Will Relieve Roll-On by

Drug Labeling and Warnings

Will Relieve Roll-On by is a Otc medication manufactured, distributed, or labeled by Will Perform, PBC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Lidocaine HCl 4%

Purpose

Topical Analgesic

Use

temporary relief of pain

Warnings

For external use only

Flammable

• keep away from excessive heat or open flame

Do not use

• on large areas of the body or on a cut, irritated or swollen skin
• on puncture wounds
• for more than one week without consulting a doctor

When using this product

• use only as directed. Read and follow all directions and warnings on this carton
• do not allow contact with eyes and mucous membranes
• do not bandage or apply local heat (such as heating pads) or medicated patch to the area of use
• do not use at the same time as other topical analgesics

Stop use and ask a doctor if

• conditions worsen
• redness is present
• irritation develops
• symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding,

• ask a healthcare professional before use

Keep out of reach of children and pets

• if swallowed, get medical help or contact a Poison Control Center right away

Directions

adults and children over 12 years:

• apply a thin layer over the affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

children 12 years or younger:

• ask a doctor

Inactive Ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., aminomethyl propanol, angelica polymorpha sinensis root extract, arnica montana flower extract, bisabolol, caprylic/capric triglyceride, capryloyl glycerin/sebacic acid copolymer, diheptyl succinate, fragrance, glycerin, water

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Distributed by Will Perform, PBC, 4040 Civic Center Drive, #200, San Rafael, CA 94903

PRINCIPAL DISPLAY PANEL - 88 mL Bottle Carton

WILL™
PERFORM
BY SERENA WILLIAMS

FAST ACTING

PAIN RELIEF
ROLL-ON
lidocaine

3 FL OZ (88 mL)

INGREDIENTS AND APPEARANCE

WILL RELIEVE ROLL-ON 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82630-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Lidocaine Hydrochloride (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	3.2 g  in 88 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
Alcohol (UNII: 3K9958V90M)
Glycerin (UNII: PDC6A3C0OX)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
LEVOMENOL (UNII: 24WE03BX2T)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
Arnica Montana Flower (UNII: OZ0E5Y15PZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82630-002-01	1 in 1 CARTON	08/01/2022
1		88 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/01/2022

Labeler - Will Perform, PBC (118584310)