SOS RITUALS PORE POP FIZZ MASK BLACKHEAD TREATMENT- salicylic acid lotion

SOS Rituals Pore Pop Fizz Mask Blackhead Treatment by

Drug Labeling and Warnings

SOS Rituals Pore Pop Fizz Mask Blackhead Treatment by is a Otc medication manufactured, distributed, or labeled by I World LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Salicylic Acid 1.1%

Purpose

Acne Treatment

Uses

For treatment of acne.

Warnings

For external use only.

Do not use

• on damaged or broken skin.

When using this product

• Keep out of eyes. Rinse with water to remove.

Stop use and ask doctor if

• rash occurs.

Keep out of reach of children.

• If product is swallowed get medical help or contact a poison control center right away.

Directions

• Clean the skin thoroughly before applying this product.
• Apply to areas of congestion, and allow 3-5 minutes to fully activate.
• Rinse thoroughly with tepid water, and follow with your moisturizer.

Other information

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

WATER (AQUA), KAOLIN, DISILOXANE, GLYCERIN, DIPROPYLENE GLYCOL, COCAMIDOPROPYL BETAINE, DISODIUM COCOYL GLUTAMATE, BETAIN, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SODIUM HYDROXIDE, 1,2-HEXANEDIOL, HYDROXYACETOPHENONE, XANTHAN GUM, POLYSORBATE 20, BUTYLENE GLYCOL, SODIUM CHLORIDE, FRAGRANCE (PARFUM), DIMETHICONE, FORSYTHIA SUSPENSA FRUIT EXTRACT, PUERARIA LOBATA ROOT EXTRACT, ANEMARRHENA ASPHODELOIDES ROOT EXTARCT, CAPRYLYL GLYCOL PENITYLRNR GLYCOL, CARAMEL, TURPENTINE, PINENE.

Questions or comments?

1-212-244-5170

Pacakge Labeling:

INGREDIENTS AND APPEARANCE

SOS RITUALS PORE POP FIZZ MASK BLACKHEAD TREATMENT 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	11 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
KAOLIN (UNII: 24H4NWX5CO)
DISILOXANE (UNII: D7M4659BPU)
GLYCERIN (UNII: PDC6A3C0OX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
BETAINE (UNII: 3SCV180C9W)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIMETHICONE (UNII: 92RU3N3Y1O)
FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)
PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
ANEMARRHENA ASPHODELOIDES ROOT (UNII: U0OC9BJL0I)
CARAMEL (UNII: T9D99G2B1R)
TURPENTINE (UNII: XJ6RUH0O4G)
PINENE (UNII: 996299PUKB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-008-00	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	02/07/2025

Labeler - I World LLC (830590126)