SYNC QUADRA- methyl salicylate, menthol, capsaicin, methyl nicotinate patch

Sync Quadra by

Drug Labeling and Warnings

Sync Quadra by is a Otc medication manufactured, distributed, or labeled by iON Pharma, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Drug facts
Active ingredients (in each patch)...... Purpose
Menthol 10% ............................................. Topical analgesic
Methyl salicylate 15% .............................. Topical analgesic
Capsaicin 0.025% ................................. Topical analgesic
Methyl nicotinate 1% ............................. Topical analgesic

Uses section

Uses:

Temporarily relieves minor aches and pains of muscles & joints associated with:

• Strains
• Sprains
• Simple Backache
• Arhtritis
• Bruises

NSAID warning, Do not use section

For external use only
Stomach bleeding warning: This product contains a NSAID, which may cause stomach bleeding. The chance is small but higher if you:

• are age 60 or older
• have had stomach ulcers or bleeding problems
• take a blood thinning (anticoagulant) or steroid drug
• take other drugs containing NSAID (aspirin, ibuprofen, naproxen, or others)
• have 3 or more alcoholic drinks every day while using this product

Do not use:

• on the face or rashes
• on wounds or damaged skin
• if allergic to aspirin or other NSIADs
• with a heating pad
• when sweating (such as from exercise or heat)
• any patch from a pouch that has been open 14 days or more days
• right before or after heart surgery
• do not bandage tightly

When using this product

When using this product

wash hands after applying or removing patch. Avoid contact with eyes. If eye contact occurs, rinse thoroughly with water. The risk of heart attack or stroke may increase if you use more than directed or for longer than directed.

Stop use section

Stop use and ask a doctor if

• condition worsens
• symptoms last for more than 7 days or clear up and occur again within a few days
• you experience signs of stomach bleeding, such as feeling faint, vomiting blood, or have bloody or black stools
• redness or swelling occurs
• a burning sensation occurs

If pregnant or breast-feeding section

Ask a doctor before use while breastfeeding and during the first 6 months of pregnancy. Do not use during the last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children section

If put in mouth, get medical help or contact a Poison Control Center right away. Package not child resistant. Dispose of the used patches after folding sticky ends together.

Directions section

Adults and children 10 years of age and older:

only use one patch at a time
clean and dry affected area
remove patch from backing film and apply to skin (see illustration)
apply 1 patch to the affected area or intact skin up to 36 hours
do not use more than 2 patches per day
do not use for more than 3 days in a row unless prescribed and instructed by a healthcare provider
the used patch should be removed from the skin when a new one is applied

INACTIVE INGREDIENT

Hypoallergenic acrylic adhesive

Questions or comments section

Questions or Comments:

833.711.8833

info@syncrelief.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SYNC QUADRA 
methyl salicylate, menthol, capsaicin, methyl nicotinate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82944-500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.025 g
METHYL NICOTINATE (UNII: 7B1AVU9DJN) (NIACIN - UNII:2679MF687A)	METHYL NICOTINATE	0.25 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g

Inactive Ingredients
Ingredient Name	Strength
ACRYLIC ACID (UNII: J94PBK7X8S)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82944-500-10	1 in 1 BOX	04/01/2025
1		10 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2025

Labeler - iON Pharma, LLC (118739596)