HANGOVERMD- capsicum spray

HangoverMD by

Drug Labeling and Warnings

HangoverMD by is a Homeopathic medication manufactured, distributed, or labeled by Sinol USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active Ingredients:

Capsicum 4x HPUS (Capsaicin)

Purpose:

Fast Headache Relief

Uses:

Relieves headache pain due to hangover

Warnings:

Temporary nasal tingling or burning may be felt for a few seconds
Do not use if you are allergic to any of the ingredients 
Sharing this container by more than one person may spread infection
Do not spray in or around eyes

Keep out of reach of children
If pregnant or breast feeding, consult a health professional before use

Other information:

Store between 68 to 77°F (20 to 25°C)

Directions:

Shake bottle before use
Spray 1 to 2 times into each nostril and inhale gently.
   Use up to 10x per day.

Other Ingredients:

Purified Water, Patented Nano-Silver (natural preservative) Eucalyptol, Sea Salt, and Vitamin C.

SPL UNCLASSIFIED SECTION

FAST HEADACHE RELIEF WITH ELECTROLYTES

Up to 10x FASTER than pills or liquids

RELIEF IN MINUTES

HangoverMD is a Homeopathic Drug

MD FORMULATED  ALL NATURAL

57 POST BENDER DOSES

MADE IN THE U.S.A.Distributed by:
Glacier Pharmaceuticals LLC
1309 Coffeen Avenue STE 1200 Sheridan, WY 82801

Hello@GetHangoverMD.com

"HPUS" indicates that this ingredient is officially listed in the Homeopathic Pharmacopoeia of the United States.

Packaging

INGREDIENTS AND APPEARANCE

HANGOVERMD 
capsicum spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15013-117
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG)	CAPSICUM	4 [hp_X]  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SILVER (UNII: 3M4G523W1G)
EUCALYPTOL (UNII: RV6J6604TK)
SEA SALT (UNII: 87GE52P74G)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15013-117-15	1 in 1 CARTON	03/12/2026
1		15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/12/2026

Labeler - Sinol USA, Inc. (790640606)