Active Ingredient

Lidocaine 4%

Purpose

Topical analgesic

Uses

Temporarily relieves minor pain associated with:

.Arthritis .Sprains .Simple backache

.Bruises .Muscle strains .Cramps

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 or 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 12 years of age and older: apply to the affected area not more than 3 to 4 times daily.
Children under 12 years of age : Consult a doctor

Inactive ingrdients

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

Principal Display Panel

NDC 73332-001-01

FOR EXTERNAL USE ONLY

CBD Pain Cream

+ Lidocaine

Label

CBD PAIN CREAM
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73332-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALLANTOIN (UNII: 344S277G0Z)
TRICAPRIN (UNII: O1PB8EU98M)
PAPRIKA (UNII: X72Z47861V)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
CANNABIS SATIVA SEED (UNII: QE567Z26NG)
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 (2500000 MW) (UNII: 05I15JNI2J)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
GRAPE SEED OIL (UNII: 930MLC8XGG)
XANTHAN GUM (UNII: TTV12P4NEE)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73332-001-01	74 mL in 1 TUBE; Type 0: Not a Combination Product	09/18/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part346	09/18/2019

Labeler - NATURES ORGANICS LLC (117141162)

Name	Address	ID/FEI	Business Operations
Establishment
Ion Labs Inc		106499791	manufacture(73332-001)

Drug Facts