SUNSET NOVELTIES HERQUAKE- numbing lubricant liquid

Sunset Novelties Herquake by

Drug Labeling and Warnings

Sunset Novelties Herquake by is a Otc medication manufactured, distributed, or labeled by Private Label Productions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Lidocaine HCI 3.5%

Purpose

External Analgesic

Use

For temporary relief of pain, soreness or burning in the perianal area.

Warnings

For external use only. Do not use this product with a mechanical device.

Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Do not exceed the daily recommended dosage.

In case of any bleeding, discontinue use and consult a doctor.

Keep this and all drugs out of reach of children. In case of accidential overdose, seek medical help or call a Poison Control Center right away.

As with any drug, consult a health care professional if you are pregnant or nursing. Ask a health care professional before using this product.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of childeren.

Directions

Apply to any area of the body where you desire extra moisture. Secure cap.

Apply externally to the affected area up to 6 times

Other information

Store at 20-25°C (68-77°F)

Inactive ingredients

Purified Water, Glycerin, Propylene Glycol, Hydroxyethylcellulose, Sodium Benzoate, Potassium Sorbate, Citric Acid

Package Label - Principal Display Panel

118 mL NDC: 77632-121-11

INGREDIENTS AND APPEARANCE

SUNSET NOVELTIES HERQUAKE 
numbing lubricant liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77632-121
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	3.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77632-121-11	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/01/2025

Labeler - Private Label Productions LLC (046278265)