KILLA ACNE EXTRA STRENGTH 2 PACK- salicylic acid patch

Killa Acne Extra Strength 2 pack by

Drug Labeling and Warnings

Killa Acne Extra Strength 2 pack by is a Otc medication manufactured, distributed, or labeled by ZitSticka, Inc., Raphas. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2%

ASK DOCTOR

Ask a doctor if irritation become severe.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a posion Control Center right away.

PURPOSE

Uses:

• For the management of acne.
• Penetrates pores to eliminate most blemishes.

INACTIVE INGREDIENT

Sodium Hyaluronate, phytosphingosine HCl, Niacinamide, Oligopeptide-10, Glycolic Acid, Madecassoside, 4-Butylresorcinol

Uses

• For the management of acne.
• Penetrates pores to eliminate most blemishes.

Directions and How to Use

How to open:

1. To remove a patch, peel the front, top corner and pull towards the center.

2. Inside, you'll find a white tab with a slit on one side. Tear along that seam to reveal the KILLA ACNE Extra Strength patch.

How to use:

1. Cleanse skin thoroughly before applying the product.

2. Once dry, apply KILLA ACNE Extra Strength pimple patch onto zit.

3. Leave on for 2+ hrs for microdarts to dissolve (for best results leave on overnight).

WARNINGS

For external use only.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KILLA ACNE EXTRA STRENGTH 2 PACK 
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81746-899
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.0125 mg  in 0.6216 mg

Inactive Ingredients
Ingredient Name	Strength
4-BUTYLRESORCINOL (UNII: 2IK4UQ3ZGA)
PHYTOSPHINGOSINE HYDROCHLORIDE (UNII: TT871XV7TU)
GLYCOLIC ACID (UNII: 0WT12SX38S)
OLIGOPEPTIDE-10 (UNII: Q46328TRNK)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
NIACINAMIDE (UNII: 25X51I8RD4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81746-899-00	1660 mg in 1 BOX; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	08/30/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M006	05/26/2023

Labeler - ZitSticka, Inc. (117778611)

Establishment
Name	Address	ID/FEI	Business Operations
Raphas		695914964	manufacture(81746-899)