Home NDC 24286-1557 Earths Care Acne Spot Treatment
Product NDC 24286-1557
11-digit product format 242861557
Labeler code 24286
Product ID 24286-1557_35338f9b-4431-c386-e063-6294a90a7aef
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form CREAM
Route TOPICAL
Labeler DLC Laboratories, Inc.
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-01-18
Substance SULFUR
Active strength 10 g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Earths Care Acne Spot Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 10 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053330 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 24286-1557-1 Earths Care Acne Spot Treatment 1 in 1 BOX CREAM 1 6 24286-1557-1 Earths Care Acne Spot Treatment 27 g in 1 TUBE CREAM 27 6 24286-1557-2 Earths Care Acne Spot Treatment 2.8 g in 1 POUCH CREAM 2.8 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SULFUR ACTIVE INGREDIENT 70FD1KFU70 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 SULFUR ACTIVE MOIETY 70FD1KFU70 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 BENTONITE INACTIVE INGREDIENT A3N5ZCN45C EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 CETEARYL GLUCOSIDE INACTIVE INGREDIENT 09FUA47KNA EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 GLYCERYL MONOSTEARATE INACTIVE INGREDIENT 230OU9XXE4 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 HYDROGENATED CASTOR OIL INACTIVE INGREDIENT ZF94AP8MEY EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 OATMEAL INACTIVE INGREDIENT 8PI54V663Y EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 PHENOXYETHANOL INACTIVE INGREDIENT HIE492ZZ3T EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 POTASSIUM SORBATE INACTIVE INGREDIENT 1VPU26JZZ4 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 SHEA BUTTER INACTIVE INGREDIENT K49155WL9Y EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 SODIUM STEAROYL GLUTAMATE INACTIVE INGREDIENT 65A9F4P024 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 SUNFLOWER OIL INACTIVE INGREDIENT 3W1JG795YI EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24286-1557 EARTHS CARE ACNE SPOT TREATMENT (SULFUR) CREAM [DLC LABORATORIES, INC.] 6 Current NDC, Legacy NDC, 3 package rows 20250519_85dab75e-5436-4e31-9ce2-c1995fde1dd9.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 42 of 54 · 1,079 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 24286-1557-1 24286155701 1 TUBE in 1 BOX (24286-1557-1) / 27 g in 1 TUBE 1 tube 2013-01-18 0000-00-00 No No Current 24286-1557-2 24286155702 2.8 g in 1 POUCH (24286-1557-2) 2.8 g 2013-01-18 0000-00-00 No No Current