Home NDC 62032-070 NU-DERM PHYSICAL UV
Product NDC 62032-070
11-digit product format 620320070
Labeler code 62032
Product ID 62032-070_2af9c0fa-9906-47c1-84af-3ed7c0a78cdc
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Obagi Cosmeceuticals LLC
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2004-01-01
Marketing end 0000-00-00
Substance ZINC OXIDE
Active strength 185 mg/g
NDC exclude flag No
Listing certified through 2020-12-31
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 · 18 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 62032-070-18 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 62032-070-18 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 62032-070-18 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 62032-070-18 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 62032-070-18 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 62032-070-18 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 62032-070-18 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 62032-070-18 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 62032-070-18 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ZINC OXIDE ACTIVE INGREDIENT SOI2LOH54Z NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 ZINC OXIDE ACTIVE MOIETY SOI2LOH54Z NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 ALPHA-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 BUTYLENE GLYCOL INACTIVE INGREDIENT 3XUS85K0RA NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) INACTIVE INGREDIENT 035JKJ76MT NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP INACTIVE INGREDIENT 08H094218D NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 ETHYLHEXYL STEARATE INACTIVE INGREDIENT EG3PA2K3K5 NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 GLYCERETH-26 INACTIVE INGREDIENT NNE56F2N14 NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 HYDROGENATED CASTOR OIL INACTIVE INGREDIENT ZF94AP8MEY NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 ISOPROPYL PALMITATE INACTIVE INGREDIENT 8CRQ2TH63M NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 TRIETHOXYCAPRYLYLSILANE INACTIVE INGREDIENT LDC331P08E NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1 YELLOW WAX INACTIVE INGREDIENT 2ZA36H0S2V NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OMP, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-070 NU-DERM PHYSICAL UV BROAD SPECTRUM SPF 32 (ZINC OXIDE) LOTION [OBAGI COSMECEUTICALS LLC] 3 Legacy NDC 20190124_0960cb9d-413e-4eeb-83b8-135b75642f90.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-070-18 62032007018 57 g in 1 BOTTLE, PLASTIC (62032-070-18) 57 g 2004-01-01 0000-00-00 No No Current