BYOMA ACNE CLEARING BODY WASH- salicylic acid liquid

Byoma Acne Clearing Body Wash by

Drug Labeling and Warnings

Byoma Acne Clearing Body Wash 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

• skin irritation occurs or gets worse.

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), Ammonium Lauryl Sulfate, Hamamelis Virginiana (Witch Hazel) Water, Cocamidopropyl Betaine, Propylene Glycol, Glycerin, Sodium Chloride, Ethyl Linoleate, Benzyl Alcohol, Sodium Hydroxide, Hydroxypropyl Guar Hydroxypropyltrimonium Chloride, Sodium Benzoate, Phytosphingosine, Ceramide NP, Citric Acid, Bakuchiol, Phenoxyethanol, Propanediol, Glucomannan, Xylitylglucoside, Anhydroxylitol, Rutin, Hydroxycinnamic Acid, Xylitol, Rhamnose, Glucuronic Acid, Glucose.

Questions or Comments?

Contact hello@byoma.com

Product Labeling

INGREDIENTS AND APPEARANCE

BYOMA ACNE CLEARING BODY WASH 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84821-005
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)
GLUCOSE (UNII: 5SL0G7R0OK)
WATER (UNII: 059QF0KO0R)
BAKUCHIOL (UNII: OT12HJU3AR)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
RHAMNOSE (UNII: QN34XC755A)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
HYDROXYPROPYL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: MVW5LK6LFT)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
GLYCERIN (UNII: PDC6A3C0OX)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
HYDROXYCINNAMIC ACID (UNII: IBS9D1EU3J)
XYLITOL (UNII: VCQ006KQ1E)
GLUCURONIC ACID (UNII: 8A5D83Q4RW)
RUTIN (UNII: 5G06TVY3R7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PROPANEDIOL (UNII: 5965N8W85T)
CERAMIDE NP (UNII: 4370DF050B)
GLUCOMANNAN (UNII: 36W3E5TAMG)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84821-005-01	400 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)