RITUAL TATTOO- lidocaine, tetracaine, witch hazel spray

Ritual Tattoo by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredients

Lidocaine 4%

Tetracaine 1%

Witch Hazel 30%

Purpose

Lidocaine: Topical analgesic

Tetracaine: Topical analgesic

Witch Hazel: Astringent

Uses

• For temporary relief of pain during tattoo and piercing procedures.
• To reduce inflammation & redness causing less damage to skin during tattooing­ or piercing procedures. Also used to desensitize the tattoo area for longer tattoo sessions and happier clients.

Warnings

• For external use only.
• If swallowed, get medical help or contact Poison Control Center. 1-800-222-1222

Do Not Use

DO NOT USE more than 2 oz. 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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

• Recommended usage is 1-2 sprays per 3 in. x 3 in. area. Reapply as needed.
• Best results if you wrap the area and let sit for 10-20 minutes.

Other Information or Comments

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

Inactive Ingredients

Benzoic acid, Distilled water

Principal Display Panel

60 mL NDC: 82171-002-60

INGREDIENTS AND APPEARANCE

RITUAL TATTOO 
lidocaine, tetracaine, witch hazel spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82171-002
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	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZOIC ACID (UNII: 8SKN0B0MIM)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82171-002-60	60 mL in 1 BOTTLE, SPRAY; 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(82171-002)