RITUAL TATTOO REVEAL FOAM- lidocaine, tetracaine, witch hazel liquid

Ritual Tattoo Reveal Foam by

Drug Labeling and Warnings

Ritual Tattoo Reveal Foam by is a Otc medication manufactured, distributed, or labeled by MK Laboratory. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Lidocaine 2% w/v. Purpose: Topical analgesic

Tetracaine 1% w/v. Purpose: Topical analgesic

Witch Hazel 30% w/v. Purpose: Astringent

Purpose

Lidocaine 2% w/v. Purpose: Topical analgesic

Tetracaine 1% w/v. Purpose: Topical analgesic

Witch Hazel 30% w/v. Purpose: Astringent

Uses

• For temporary relief of pain during tattoo and piercing procedures.
• Reduce sensitivity, inflammation, and redness during tattoo and piercing aftercare

Warnings

• For external use only.
• Check with client for history of allergic reactions to topical analgesics.

DO NOT USE

DO NOT USE more than 30 mL in a 6 hour period.

WHEN USING

• Avoid contact with eyes. In case of eye contact, flush eyes with water.

STOP USE

• Stop use and contact doctor if skin irritations occur. If irritation, rinse thoroughly with water.
• If swallowed, get medical help or contact Poison Control Center. 1-800-222-1222

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Directions

• Pump foam generously, spread over tattoo or piercing and let sit 10-30 seconds before wiping with damp paper towel.
• For use during breaks and on completed tattoos and piercing. Also great for aftercare uses.

Other Information or Comments

For questions or comments please send email to Ritualtattooproducts@gmail.com

Inactive Ingredients

Cannabis Sativa Seed Oil (Hempseed Oil), Citric Acid, Coconut Oil, Glycerin, Hydroxide Pellets, Jojoba Oil, Olea Europaea Fruit Oil, Palm Kernel Flakes, Potassium, Tocopheryl Acetate (Vitamin E Oil), Water

Principal Display Panel

250 mL NDC: 82171-003-60

INGREDIENTS AND APPEARANCE

RITUAL TATTOO REVEAL FOAM 
lidocaine, tetracaine, witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82171-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV)	TETRACAINE	1 g  in 100 mL
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	30 g  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PALM KERNEL OIL (UNII: B0S90M0233)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
JOJOBA OIL (UNII: 724GKU717M)
WATER (UNII: 059QF0KO0R)
COCONUT OIL (UNII: Q9L0O73W7L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82171-003-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2021

Labeler - MK Laboratory (118238452)

Establishment
Name	Address	ID/FEI	Business Operations
MK Laboratory		118238452	manufacture(82171-003)