Label: ADULT ACNOMEL- resorcinol, sulfur cream
- NDC Code(s): 69846-911-61
- Packager: NUMARK BRANDS, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 3, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use on:
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive 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 or peeling occurs, reduce application to once a day or every other day
- Other information
- Inactive ingredients
- Questions?
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PRINCIPAL DISPLAY PANEL
NO Benzoyl
Peroxide
For clear, healthy-looking skin
ADULT ACNOMEL ®
Tinted Cream
DERMATOLOGIST RECOMMENDED
Acne Spot Treatment
NET WT.
1.3 OZ.
(36 GRAMS)
TRUSTED
SINCE 1948
• Less drying- does not contain Benzoyl Peroxide
• Effective treatment for adult acne & blemishes
• Helps improve skin texture affected by Rosacea
with 8%
Sulfer
Clears up acne pimples
and helps prevent new
ones from forming
Distributed by:
Numark Brands
138 East Main St, Suite 201
Kent, OH 44240
1-800-214-2379
07/24
30% More
ADULT ACNE
Medication
For clear, healthy-looking skin
ADULT ACNOMEL©
Tinted Cream
NET WT. 1.3 OZ. (36 GRAMS)
Distributed by Numark Brands, 27070 Miles Rd, Solon OH 44139 1-800-214-2379
D14048 Rev 7/19

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INGREDIENTS AND APPEARANCE
ADULT ACNOMEL
resorcinol, sulfur creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69846-911 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 20 mg in 1 g SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 80 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BENTONITE (UNII: A3N5ZCN45C) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) FERRIC OXIDE RED (UNII: 1K09F3G675) OCTOXYNOL-9 (UNII: 7JPC6Y25QS) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69846-911-61 1 in 1 CARTON 10/08/1946 1 36 g 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 10/08/1946 Labeler - NUMARK BRANDS, INC (080184668)
