Home NDC 52810-103 EXTRA DRAWING ACNE RELIEF
Product NDC 52810-103
11-digit product format 528100103
Labeler code 52810
Product ID 52810-103_d387e675-bf13-3921-e053-2995a90ad42e
Type HUMAN OTC DRUG
Nonproprietary name MAHONIA AQUIFOLIUM, CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, SAMBUCUS NIGRA, THUJA OCCIDENTALIS
Dosage form SALVE
Route TOPICAL
Labeler PUREMEDY
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-06-13
Marketing end 0000-00-00
Substance MAHONIA AQUIFOLIUM FRUITING TOP; CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; SAMBUCUS NIGRA FLOWER; THUJA OCCIDENTALIS LEAF
Active strength 1 [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 52810-103-12 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 52810-103-13 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 52810-103-12 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 52810-103-13 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 52810-103-53 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 52810-103-52 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 52810-103-53 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 52810-103-52 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52810-103-12 EXTRA DRAWING ACNE RELIEF 28 g in 1 JAR SALVE 28 5 52810-103-13 EXTRA DRAWING ACNE RELIEF 56 g in 1 JAR SALVE 56 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52810-103 EXTRA DRAWING ACNE RELIEF (MAHONIA AQUIFOLIUM, CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, SAMBUCUS NIGRA, THUJA OCCIDENTALIS) SALVE [PUREMEDY] 5 Legacy NDC, 2 package rows 20240112_3e8dfa74-8e63-41e4-a4d3-c6cfa805b215.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52810-103-12 52810010312 28 g in 1 JAR (52810-103-12) 28 g 2016-06-13 0000-00-00 No No Current 52810-103-13 52810010313 56 g in 1 JAR (52810-103-13) 56 g 2016-06-13 0000-00-00 No No Current