SEYTU SPOT- salicylic acid gel

SEYTU Spot by

Drug Labeling and Warnings

SEYTU Spot by is a Otc medication manufactured, distributed, or labeled by Omnilife USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment Gel

Uses

• For the treatment of acne
• Reduce the severity of new acne pimples, blackheads, or whiteheads

Warnings

• For external use only
• If experience skin irritation or prolonged stinging, stop using the product and consult your physician

When using this product

• skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time
• Follow the use instructions on the label
• Do not exceed the recommended applications

Keep out of reach of children.

• If swallowed, get medical help or contact a poison control center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Directions

• Clean the skin thoroughly before applying this product
• Cover the entire affected area with a thin layer one to three times daily
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other Information

Do not use if the security seal has been broken

Inactive Ingredients

Alcohol Denat., Allantoin, Ammonium Polyacryloyldimethyl Taurate, Bacillus Ferment Filtrate Extract, Butylene Glycol, Ethylhexylglycerin, Madecassoside, Phenoxyethanol, Portulaca Oleracea Extract, Propylene Glycol, Sodium Hydroxide, Tetrasodium EDTA, Water (Aqua).

Questions?

CUSTOMER SERVICE: U.S.A. 1 844 847 3988.
seytu.omnilife.com

Principal Display Panel

SEYTÚ®

SYSTEM
SPOT-SPECIALIST

Spot Gel
Gel Localizado
Acne Treatment

Salicylic Acid 2%
Ácido Salicílico 2%
Postbiotics
Postbióticos
Madecassoside

0.5 fl Oz. (15 mL)


MADE IN USA WITH
GLOBALLY SOURCED
INGREDIENTS

PRODUCT NOT TESTED
ON ANIMALS

HYPOALLERGENIC
PRODUCT

IMPORTED AND / OR DISTRIBUTED BY:
OMNILIFE USA, INC. 3900 SOUTH
FREEWAY, FORT WORTH, TX 76110.

Label

INGREDIENTS AND APPEARANCE

SEYTU SPOT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84271-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALLANTOIN (UNII: 344S277G0Z)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PURSLANE (UNII: M6S840WXG5)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84271-002-00	1 in 1 CARTON	12/01/2024
1		15 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 Drug	M006	12/01/2024

Labeler - Omnilife USA, Inc. (160551441)