JACK BLACK BUMP FIX- salicylic acid liquid

Jack Black Bump Fix by

Drug Labeling and Warnings

Jack Black Bump Fix by is a Otc medication manufactured, distributed, or labeled by Jack Black, L.L.C., Swiss-American CDMO, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Keep out of reach of children

Keep out of reach of children

Uses

For the management of acne.  Helps clear acne blemishes and blackheads and allows skin to heal.  Helps prevent new acne blemishes and blackheads form forming.

Uses

For the management of acne.  Helps clear acne blemishes and blackheads and allows skin to heal.  Helps prevent new acne blemishes and blackheads form forming.

Directions

Clean the skin thoroughly before applying this product.  Cover the entire affected area with a think layer one to three times daily.  Because excesssive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.  If bothersome dryness orpeeling occurs, reduce application to once a day or every other day.

Active Ingredient

Salicylic Acid   2%

Inactive Ingredients

water, alcohol denatured, propylene glycol, lactic acid, sodium bicarbonate, methyl glyceth-20, sodium bisulfite, sorbic acid, disodium EDTA, sodium hyaluronate, glycerin, allantoin, aloe barbadensis leaf, galactoarabinan, butylene glycol, hamamelis virginiana (witch hazel) extract, camellia sinensis leaf extract, chamomilla recutita(matricaria) flower extract, epilobium angustifolium flower/leaf/stem extract

Questions

Questions? 1-877-766-3388

1-469-341-2700

www.getjackblack.com

Labeling

INGREDIENTS AND APPEARANCE

JACK BLACK BUMP FIX 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66738-022
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 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LACTIC ACID (UNII: 33X04XA5AT)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
SODIUM BISULFITE (UNII: TZX5469Z6I)
SORBIC ACID (UNII: X045WJ989B)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYALURONIC ACID (UNII: S270N0TRQY)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GALACTOARABINAN (UNII: SL4SX1O487)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CHAMOMILE (UNII: FGL3685T2X)
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66738-022-01	183 g in 1 BOTTLE; Type 0: Not a Combination Product	09/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	09/09/2020

Labeler - Jack Black, L.L.C. (847024036)

Registrant - Swiss-American CDMO, LLC (080170933)

Establishment
Name	Address	ID/FEI	Business Operations
Swiss-American CDMO, LLC		080170933	manufacture(66738-022)