CBD PAIN CREAM- lidocaine cream

CBD pain cream by

Drug Labeling and Warnings

CBD pain cream by is a Otc medication manufactured, distributed, or labeled by NATURES ORGANICS LLC, Ion Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

STORAGE AND HANDLING

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.

QUESTIONS

Principal Display Panel

NDC: 73332-001-01

FOR EXTERNAL USE ONLY

CBD Pain Cream

+ Lidocaine

INGREDIENTS AND APPEARANCE

CBD PAIN CREAM 
lidocaine cream

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

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

Labeler - NATURES ORGANICS LLC (117141162)

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