CANNAFLEX- trolamine salicylate cream

Cannaflex by

Drug Labeling and Warnings

Cannaflex by is a Otc medication manufactured, distributed, or labeled by ALLURE LABS INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Trolamine Salicylate - 10%

PURPOSE

Purpose:

Topical Analgesic

INDICATIONS & USAGE

Uses: Temporarily relieves minor pain associated with arthritis, backache, muscle strains, muscle sprains, bruises, cramps. 

WARNINGS

Warning: For external use only.

ASK DOCTOR

Allergy alert if prone to allergic reaction from aspirin or salicylates, consult a Doctor before use.

WHEN USING

When using this product: Use only as directed. Read and follow all directions and warnings on this label. Do not bandage tightly or use with a heated pad. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged, broken or irritated skin. Do not use at the same time with other topical analgesics.

STOP USE

Stop use and ask a doctor if condition worsens. Symptoms persist for more than 7 days or clear up and occur again within a few days. Redness is persistent. Irritation develops.

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Inactive ingredients: Water, Coconut Alkanes, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Methyl Sulfonyl Methane, Stearic Acid, Glycerin, Aesculus Hippocastannum (Horse Chestnut) Seed Extract, Rosa Moschata Seed Oil, Menthoxypropanediol, Sorbitan Olivate, Cannabidiol (From full spectrum hemp extract), Medium Chain Triglyceride, Cetearyl Olivate, Phenoxyethanol, Menthyl Lactate, Tocopherol, Mentha Piperita (Pepperment) Oil, Cetyl Palmitate, Sorbitan Palmitate, Coco-Caprylate/Caprate, Caprylyl Glycol, Menthol, Xanthan Gum, Ethylhexylglycerin, Hexylene Glycol, Vanillyl Butyl Ether.

DOSAGE & ADMINISTRATION

Adults and Children over 12 years: Apply generously to affected area. Massage into painful area until thoroughly asborbed into skin. Repeat as necessary, But no more than 4 times daily.

QUESTIONS

Questions or Comments? 

Call our customer service department at: 1-800-898-5153 

PRINCIPAL DISPLAY PANEL

Manufactured for:

CBD Therapeutics, LLC

Salt Lake City, UT 84116

INGREDIENTS AND APPEARANCE

CANNAFLEX 
trolamine salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4177
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ)	TROLAMINE SALICYLATE	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCONUT ALKANES (UNII: 1E5KJY107T)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERIN (UNII: PDC6A3C0OX)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
ROSA MOSCHATA SEED OIL (UNII: T031ZE559T)
3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CANNABIDIOL (UNII: 19GBJ60SN5)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
TOCOPHEROL (UNII: R0ZB2556P8)
PEPPERMINT OIL (UNII: AV092KU4JH)
CETYL PALMITATE (UNII: 5ZA2S6B08X)
SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
MENTHOL (UNII: L7T10EIP3A)
XANTHAN GUM (UNII: TTV12P4NEE)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4177-2	1 in 1 CARTON	10/16/2019
1	NDC: 62742-4177-1	45 mL in 1 TUBE; 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	10/16/2019

Labeler - ALLURE LABS INC. (926831603)

Registrant - ALLURE LABS INC. (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
ALLURE LABS INC.		926831603	manufacture(62742-4177)