SYREN INTIMATE PAIN RELIEF- lidocaine hydrochloride gel

SYREN INTIMATE PAIN RELIEF by

Drug Labeling and Warnings

SYREN INTIMATE PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Icon Health Science, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Lidocaine hydrochloride 4%

Purpose

Topical Analgesic

Uses:

• For the temporary relief of pain (and itching) associated with minor, burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations.

Warnings:

For external use only.

Do not use

• in large quantities, particularly over raw surfaces or blistered areas.

When using this product

• Avoid contact with the eyes

Stop use and ask a doctor if

• condition worsens, or if symptoms persist for more than 7 days or 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. 

If pregnant or breast-feeding,

ask a health professional before use

Directions:

• Adults and children 2 years of age or older:  Apply to affected area not more than 3 to 4 times daily.
• Children under 2 years of age:  consult a doctor.

Other information:

• Store at 20-25°C (68-77°F) and protect from moisture.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Benzoic Acid, Cannabis Sativus (Hemp) Seed Oil, Carbomer, Carrageenan, Ethylhexylglycerin, I-Arginine, PEG-8, Phenoxyethanol, Polysorbate-20, Propylene Glycol, Tocopherol Acetate (Vitamin E), Triethanolamine.

Questions?

(800) 243-8370

Package Labeling:

INGREDIENTS AND APPEARANCE

SYREN INTIMATE PAIN RELIEF 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69233-122
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BENZOIC ACID (UNII: 8SKN0B0MIM)
HEMP (UNII: TD1MUT01Q7)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CARRAGEENAN (UNII: 5C69YCD2YJ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ARGININE (UNII: 94ZLA3W45F)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69233-122-02	1 in 1 BOX	01/10/2020
1		60 mL in 1 JAR; 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	01/10/2020

Labeler - Icon Health Science, LLC (079435759)