B PURE BLEMISH CONCEALER FOR ACNE PRONE SKIN NUDE- salicylic acid cream

b pure Blemish Concealer for Acne Prone Skin Nude by

Drug Labeling and Warnings

b pure Blemish Concealer for Acne Prone Skin Nude by is a Otc medication manufactured, distributed, or labeled by Fourstar Group USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic Acid 0.5%

Purpose

Acne medication

Uses

For the treatment of acne.

Warnings

For external use only.

When using this product

• If using other topical acne medicines, dryness and skin irritation can occur.
• Discontinue use if irritation occurs.
• Do not use this product around the eye area.

Stop use and ask a doctor if

• rectal bleeding occurs.
• condition worsens or does not improve within 7 days.

Keep out of reach of children.

Directions

• apply to clean skin.
• apply to the temples, brows bones, cheekbones, and affected areas.
• blend with your fingers for a clean, sculpted look.

Other information

Store at room temperature.

Inactive ingredients

water, isododecane, ethylhexyl palmitate, propylene glycol, glycerin, lauryl dimethicone, polyglyceryl-2 diisostearate, c12-15 alkyl benzoate, hydrogenated polyisobutene, microcrystalline wax, quaternium-18 bentonite, peg-10 dimethicone, peg-30 dipolyhydroxystearate, magnesium stearate, magnesium sulfate, phenoxyethanol, chlorphenesin, ethylhexylglycerin, tocopheryl acetate, disodium edta, titanium dioxide, iron oxides

Questions?

1-800-639-3803 Weekdays 9 AM to 4 PM EST

Call toll-free 508-473-7688 or visit www.foustari.com

Package Labeling:

INGREDIENTS AND APPEARANCE

B PURE BLEMISH CONCEALER FOR ACNE PRONE SKIN NUDE 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80684-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISODODECANE (UNII: A8289P68Y2)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
BENTOQUATAM (UNII: 7F465U79Q1)
PEG-30 DIPOLYHYDROXYSTEARATE (4000 MW) (UNII: 9713Q0S7FO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80684-108-00	1.4 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/01/2024

Labeler - Fourstar Group USA, Inc. (140099503)