SUNMED MOTION- lidocaine liquid 
Sunflora Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SUNMED MOTION

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.

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

image description

SUNMED MOTION 
lidocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73240-902
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73240-902-111 in 1 BOX08/22/2019
174 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/22/2019
Labeler - Sunflora Inc (067153368)

Revised: 8/2019
Document Id: ab6d01ad-61f7-438b-ae5b-57ab51156bb6
Set id: 1ef36715-2b45-441e-9f61-d99b8d553d11
Version: 1
Effective Time: 20190822
 
Sunflora Inc