ACNE CONTROL- cream cream 
Walgreen

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Acne Control Cleanser

Active Ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Uses

For the treatment of acne.

Warnings

For external use only.

When using this product

  • Skin irritation and drynessis 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.

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Sensitivity Test for a New user. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated.

Inactive Ingredients

Water (Aqua), Cocamidopropyl hydroxysultaine, Glycerin, Sodiumj Lauroyl sarcosinate, Sodium Methyl Cocvoyl Taurate, PEG-150 Pentaerythrityl Tetrastearate, Niacinamide, Ceramide NP, Ceramide AP, Ceramide EOP, Carbomer, Phytosphingosine, Cholesterol, Sodium Lauroyl Lactylate, Hydrolyzed Hyaluronic Acid, Disodium EDTA, Benzyl alcohol, Ethylhexylglycerin, Tocopherol, Xanthan gum, Citric Acid, Sodium Hydroxide.

Label Copy

Principal Display Panel

ACNE CONTROL 
cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5834
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2000 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER 940 (UNII: 4Q93RCW27E)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
TOCOPHEROL (UNII: R0ZB2556P8)  
WATER (UNII: 059QF0KO0R)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
CERAMIDE AP (UNII: F1X8L2B00J)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
NIACINAMIDE (UNII: 25X51I8RD4)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
CERAMIDE 1 (UNII: 5THT33P7X7)  
HYALURONIC ACID (UNII: S270N0TRQY)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
CERAMIDE NP (UNII: 4370DF050B)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-5834-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/11/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00609/11/2023
Labeler - Walgreen (008965063)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(0363-5834)

Revised: 9/2023
Document Id: 05ade52c-a184-087f-e063-6394a90ad7ae
Set id: fc60cccb-405b-e49e-e053-6394a90a5a12
Version: 2
Effective Time: 20230918
 
Walgreen