SUNMED MOTION- lidocaine liquid

SUNMED MOTION by

Drug Labeling and Warnings

SUNMED MOTION by is a Otc medication manufactured, distributed, or labeled by Sunflora Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Lidocaine 4%

Purpose

Topical Analgesic

Uses

Temporarily relieves minor pain associated with:

arthritis  sprains  simple backache  muscle strains  cramps  bruises

Warnings

For external use only

When using this product

use only as directed do not bandage tightly  avoid contact with eyes  do not apply to wounds or damaged skin  do not use in large  quantities, particularly over raw surfaces or blistered areas.

Stop use and ask a doctor if

condition worsens  symptoms persist for more than 7 days symptoms clear up and occur again within a few days

Keep out of reach of children

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

Directions

Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily.

Children under 2 years of age: Consult a doctor.

Inactive Ingredients

Allantoin, Caprylic/Capric Triglyceride, Capsicum Annuum Fruit Powder, Calcium Disodium EDTA, Cannabis Sativa (Aerial) Extract Oil, Dimethicone, dl-alpha Tocopheryl Acetate, Ethyl Alcohol, Ethylhexylglycerin, Ethylhexyl Stearate, Fragrance, Glycerin, Phenoxyethanol, Polysorbate 80, Propanediol, Propylene Glycol, Purified Water, Simethicone, Sodium Polyacrylate, Trideceth-6, Vitis Vinifera (Grape) Seed Oil, Xanthan Gum.

SPL UNCLASSIFIED SECTION

Visit us at SUNFLORA.org

This product has not been evaluated by the Food & Drug Administration and is not intended to diagnose, treat, cure, or prevent any disease. Consult your physician before use. For adults 18+.

DISTRIBUTED BY:

SunFlora, Inc.
411 19th street S

St.  Petersberg, FL 

Packaging

INGREDIENTS AND APPEARANCE

SUNMED MOTION 
lidocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73240-902
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PAPRIKA (UNII: X72Z47861V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
DIMETHICONE (UNII: 92RU3N3Y1O)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
ALCOHOL (UNII: 3K9958V90M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPANEDIOL (UNII: 5965N8W85T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
GRAPE SEED OIL (UNII: 930MLC8XGG)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73240-902-11	1 in 1 BOX	08/22/2019
1		74 mL in 1 BOTTLE; 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	08/22/2019

Labeler - Sunflora Inc (067153368)