Home NDC 73318-7003 SA Acne Spot Treatment
Product NDC 73318-7003
11-digit product format 733187003
Labeler code 73318
Product ID 73318-7003_4736d5b5-bdf4-d601-e063-6394a90a7bc9
Type HUMAN OTC DRUG
Nonproprietary name Acne Spot Treatment
Dosage form LOTION
Route TOPICAL
Labeler Skin PS Brands
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-07-05
Substance SALICYLIC ACID
Active strength 20 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product 73318-7003 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 73318-7003 73318-7003-9 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 SA Acne Spot Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 103568 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 73318-7003-9 SA Acne Spot Treatment 1 in 1 CARTON LOTION 1 6 73318-7003-9 SA Acne Spot Treatment 9 g in 1 BOTTLE, GLASS LOTION 9 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73318-7003 SA ACNE SPOT TREATMENT (ACNE SPOT TREATMENT) LOTION [SKIN PS BRANDS] 4 Current NDC, 2 package rows 20241228_ffc06cbd-783d-ad07-e053-6294a90af300.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 8 of 55 · 1,088 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 73318-7003-9 73318700309 1 BOTTLE, GLASS in 1 CARTON (73318-7003-9) / 9 g in 1 BOTTLE, GLASS 2023-07-05 No No Current