Home NDC 70764-201 BOTANICAL SOOTHING
Product NDC 70764-201
11-digit product format 707640201
Labeler code 70764
Product ID 70764-201_474bb04f-2be5-2dd9-e063-6394a90a6a3c
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler CONTROL CORRECTIVE SKINCARE INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-06-08
Substance OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength 6.9; 3; 4 g/100mL; g/100mL; g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 · 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 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 70764-201-52 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 BOTANICAL SOOTHING
Brand name suffix SPF-30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 6.9 g/100mL OCTISALATE 3 g/100mL ZINC OXIDE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 70764-201-22 BOTANICAL SOOTHINGSPF-30 74 mL in 1 BOTTLE CREAM 74 6 70764-201-52 BOTANICAL SOOTHINGSPF-30 1 in 1 BOX CREAM 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70764-201 BOTANICAL SOOTHING SPF-30 (OCTINOXATE, OCTISALATE, ZINC OXIDE) CREAM [CONTROL CORRECTIVE SKINCARE INC] 5 Current NDC, Legacy NDC, 2 package rows 20230923_00a923fe-e6da-420e-a705-4773ecc2176b.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 143 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Mineral Sunscreen 20% Zinc Oxide ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 31416d04-2d6f-7cf9-e063-6294a90a9806 2025-12-09 Warnings Exact identifier application number: M020 Matte Invisible Mineral Sunscreen Non-Tinted ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 3143968a-096e-b9ac-e063-6294a90ada0d 2025-12-09 Warnings Exact identifier application number: M020 Daily Mineral Sunscreen 20% Zinc Oxide ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 314299b1-a78b-c1bd-e063-6294a90ab43b 2025-12-09 Warnings Exact identifier application number: M020 Sheer Satin Mineral Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 3143d8b0-4af8-f52d-e063-6294a90a926b 2025-12-09 Warnings Exact identifier application number: M020 Matte Invisible Mineral Sunscreen ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 3142ed0f-f379-f240-e063-6294a90a5303 2025-12-09 Warnings Exact identifier application number: M020 Sheer Non-Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE Face Collection, L.L.C. 33d83cfb-045d-141c-e063-6394a90a2e04 2025-12-09 Exact identifier application number: M020 First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30 ZINC OXIDE The Procter & Gamble Manufacturing Company 45875865-5e9c-d652-e063-6394a90ad5fa 2025-12-09 Warnings Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Maloney Plastic Surgery Skin Care, PLLC 316b7584-c782-fe9e-e063-6394a90a76fe 2025-12-09 Exact identifier application number: M020 Transparent Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE Face Collection, L.L.C. 33dbfd9b-b90f-bb32-e063-6294a90af7dc 2025-12-09 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Maloney Plastic Surgery Skin Care, PLLC 316b46ac-6dde-72d1-e063-6294a90a03da 2025-12-09 Exact identifier application number: M020 Replenish ZINC OXIDE Maloney Plastic Surgery Skin Care, PLLC 316c43fb-0c15-87d4-e063-6294a90a0a63 2025-12-09 Exact identifier application number: M020 BIOJUVE Microbiome-Safe Sheer Finish SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories ece7565b-f3e5-3386-e053-2a95a90a5802 2025-12-09 Warnings Exact identifier application number: M020 Hydraboost Lip Treatment AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Bluemercury 2cf30083-8723-23f6-e063-6394a90a55de 2025-12-09 Warnings Exact identifier application number: M020 Florida Babe Sport Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Tichy Anesthesia PA 31e4756d-8604-6e75-e063-6294a90aebe1 2025-12-09 Exact identifier application number: M020 Florida Babe Sport Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Tichy Anesthesia PA 31e4d9ae-f532-f9f5-e063-6294a90a8d39 2025-12-09 Exact identifier application number: M020 Arbonne FunSun Mineral Sunscreen Broad Spectrum SPF 30 ZINC OXIDE Arbonne International, LLC 91bcd120-28e5-4f44-9522-550c1dbcd82c 2025-12-09 Warnings Exact identifier application number: M020 Florida Babe Active Tinted 20percent Zinc Oxide Mineral Sunscreen ZINC OXIDE Tichy Anesthesia PA 31e509f2-dcb6-5ae0-e063-6394a90a70c1 2025-12-09 Exact identifier application number: M020 Florida Babe Active Non-Tinted 20percent Zinc Oxide Mineral Sunscreen ZINC OXIDE Tichy Anesthesia PA 31e57817-b8c4-8178-e063-6294a90a0149 2025-12-09 Exact identifier application number: M020 Florida Babe Everyday Tinted Replenishing Daily Protection ZINC OXIDE Tichy Anesthesia PA 3231f1fe-51b3-b2e7-e063-6394a90a2758 2025-12-09 Exact identifier application number: M020 Florida Babe Everyday Tinted Replenishing Daily Protection ZINC OXIDE Tichy Anesthesia PA 31e63876-3e39-adc6-e063-6394a90ab146 2025-12-09 Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70764-201-22 70764020122 74 mL in 1 BOTTLE 74 ml Historical 70764-201-52 70764020152 1 BOTTLE in 1 BOX (70764-201-52) / 74 mL in 1 BOTTLE (70764-201-22) 1 bottle 2016-06-08 0000-00-00 No No Current