B-LUCID TARGETED BODY ACNE GEL- salicylic acid gel

B-Lucid Targeted Body Acne Gel by

Drug Labeling and Warnings

B-Lucid Targeted Body Acne Gel by is a Otc medication manufactured, distributed, or labeled by Maelys Cosmetics, LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Salicylic Acid 2%

Purpose

Acne treatment

Uses

For the treatment of acne

Warnings

For external use only.

Keep out of reach of children.

Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.  Do not get into eyes. tt excessive skin irritation develops or increases, discontinue use and consult a doctor. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply a thin layer directly to acne on the chest, booty, and other affected areas. Massage into the skin in circular motions until fully absorbed. Use twice a day for best results.

Inactive Ingredients:

Water, Glycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Propanediol, Caprylic/Capric Triglyceride, C12-C15 Alkyl Benzoate, Isostearyl Linoleate, PEG-100 Stearate, Glyceryl Stearate, Niacinamide, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Glycolic Acid, Epilobium Fleischeri Flower/Leaf/Stem Extract, Zinc PCA, Centella Asiatica Extract, Camellia Sinensis Leaf Extract, Tocopherol, Polyglyceryl-4 Caprate, Silica, Amylopectin, Sorbitan Isostearate, Parfum (Fragrance), Ethylhexylglycerin, Polydextrose, Dextrin, Phenoxyethanol, Citric Acid, Sodium Hydroxide, Coumarin, CI 42090 (Blue 1).

Other Information

Protect this product from excessive heat and direct sun.

Question or Comments:

1-800-253-1983

Package Labeling:

INGREDIENTS AND APPEARANCE

B-LUCID TARGETED BODY ACNE GEL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83010-010
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ISOSTEARYL LINOLEATE (UNII: 4778M3HR0N)
PEG-100 STEARATE (UNII: YD01N1999R)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
NIACINAMIDE (UNII: 25X51I8RD4)
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
GLYCOLIC ACID (UNII: 0WT12SX38S)
ZINC PIDOLATE (UNII: C32PQ86DH4)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TOCOPHEROL (UNII: R0ZB2556P8)
POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYDEXTROSE (UNII: VH2XOU12IE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COUMARIN (UNII: A4VZ22K1WT)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83010-010-00	1 in 1 CARTON	01/01/2023
1		100 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	01/01/2023

Labeler - Maelys Cosmetics, LTD (532018258)