TIDL PAIN RELIEF MASSAGING ROLL-ON- roll-on liniment

TIDL PAIN RELIEF MASSAGING ROLL-ON by

Drug Labeling and Warnings

TIDL PAIN RELIEF MASSAGING ROLL-ON by is a Otc medication manufactured, distributed, or labeled by The Anthos Group, THE ANTHOS GROUP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 4%,

Menthol 2.5%

PURPOSE

Topical anesthetic

INDICATIONS & USAGE

Use for the temporary relief of pain

WARNINGS

Wamings
For extemal use only .

KEEP OUT OF REACH OF CHILDREN

If pregnant or breast-feeding , ask a health professional before use . Keep out of reach of children and pets. If swallowed , get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT

Ginger Extract
Saffron Extract
Water
Mugwort Leaf Extract
Vanillyn Butyl
Borneol
Carbohydrates

Directions

Adults and children 12 years of age and older
apply a thin layer to affected area every 6-8 hours , not more han 3-4 times daily
massage until thoroughly absorbed into skin
wash hands with soap and water after each usemore than 3 to 4 times daily
Children under 12 years of age : consult a doctor

PRINCIPAL DISPLAY PANEL

79740-011-01

79740-011-02

INGREDIENTS AND APPEARANCE

TIDL PAIN RELIEF MASSAGING ROLL-ON 
roll-on liniment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79740-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.5 g  in 100 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SIALYL LEWIS A (UNII: ZEJ6FM4UJK)
GINGER (UNII: C5529G5JPQ)
CROCUS SATIVUS FLOWER (UNII: 00IF91KFKQ)
ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
ETHYL VANILLIN (UNII: YC9ST449YJ)
WATER (UNII: 059QF0KO0R)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79740-011-02	85 g in 1 BOTTLE; Type 0: Not a Combination Product	10/26/2022
2	NDC: 79740-011-01	85 g in 1 BOTTLE; Type 0: Not a Combination Product	10/26/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/26/2022

Labeler - The Anthos Group (117511051)

Establishment
Name	Address	ID/FEI	Business Operations
THE ANTHOS GROUP		117511051	manufacture(79740-011)