BYOMA ACNE CLEARING CLEANSER- salicylic acid liquid

Byoma Acne Clearing Cleanser by

Drug Labeling and Warnings

Byoma Acne Clearing Cleanser by is a Otc medication manufactured, distributed, or labeled by Byoma Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Use

• for the treatment of acne

Warnings

For external use only

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.
• rinse right away with water if it gets in eyes.

Stop use and ask a doctor if

• irritation becomes severe.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Centre right away.

Directions

• Wet the skin and gently massage for 1-2 minutes and rinse well.
• If bothersome dryness or peeling occurs, reduce frequency of use.

Other Information

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

Inactive Ingredients

Aqua (Water), Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Stearic Acid, Propylene Glycol, Cocamidopropyl Betaine, Glyceryl Stearate, Sodium Methyl Cocoyl Taurate, Sodium Hydroxide, Zinc Gluconate, Glycol Distearate, Ethyl Linoleate, Phenoxyethanol, Sodium Chloride, Camellia Sinensis (Green Tea) Leaf Extract, Coconut Acid, Ethylhexylglycerin, Allantoin, Bakuchiol, Phytosphingosine, Ceramide NP, Propanediol, Rutin, Potassium Sorbate, Hydroxycinnamic Acid, Sodium Benzoate.

Questions or Comments?

Contact hello@byoma.com

Product Labeling

INGREDIENTS AND APPEARANCE

BYOMA ACNE CLEARING CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84821-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
BAKUCHIOL (UNII: OT12HJU3AR)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCONUT ACID (UNII: 40U37V505D)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
HYDROXYCINNAMIC ACID (UNII: IBS9D1EU3J)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALLANTOIN (UNII: 344S277G0Z)
PROPANEDIOL (UNII: 5965N8W85T)
CERAMIDE NP (UNII: 4370DF050B)
GLUCOMANNAN (UNII: 36W3E5TAMG)
RUTIN (UNII: 5G06TVY3R7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84821-007-01	175 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/12/2025

Labeler - Byoma Ltd (228554984)