Home NDC 49404-153 DR.JART EVERY SUN DAY MINERAL SUN SCREEN
Product NDC 49404-153
11-digit product format 494040153
Labeler code 49404
Product ID 49404-153_47ed472b-224a-5b9a-e063-6394a90a7030
Type HUMAN OTC DRUG
Nonproprietary name Titanium dioxide, Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Have & Be Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-22
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 115; 41 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 DR.JART EVERY SUN DAY MINERAL SUN SCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 115 mg/mL TITANIUM DIOXIDE 41 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49404-153-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 1 in 1 CARTON CREAM 1 5 49404-153-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 50 mL in 1 TUBE CREAM 50 5 49404-153-02 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 5 mL in 1 TUBE CREAM 5 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49404-153 DR.JART EVERY SUN DAY MINERAL SUN SCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HAVE & BE CO., LTD.] 4 Current NDC, Legacy NDC, 3 package rows 20241227_f06c31b4-da5f-6495-e053-2995a90ae67c.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 281 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join H.E.B. Mineral Sunscreen Broad Spectrum SPF 50 TITANIUM DIOXIDE, ZINC OXIDE H.E.B. c5279caf-3af9-d163-e053-2995a90a943b 2024-10-15 Warnings Exact identifier application number: M020 HEB Face 50 Clear Zinc Sunscreen OCTOCRYLENE, ZINC OXIDE H.E.B. f6e3c883-0087-dcd6-e053-6394a90a1272 2024-10-15 Warnings Exact identifier application number: M020 HEB Mineral Sunscreen SPF 50 ZINC OXIDE H.E.B. de99343b-c74c-3f43-e053-2995a90ac9dd 2024-10-15 Warnings Exact identifier application number: M020 HEB SPF 55 Babies and Kids Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B. f5660a97-57c8-61c7-e053-2995a90a0164 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 362f726b-d52b-4dae-ade6-a47de47697ef 2024-10-15 Warnings Exact identifier application number: M020 HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face ZINC OXIDE H.E.B. dfb43fc5-4968-f999-e053-2a95a90a0819 2024-10-15 Warnings Exact identifier application number: M020 H.E.B BABY SPF 50 SUNSCREEN H.E.B 61273611-ab7a-4216-aebe-2c8d89660281 2024-10-15 Warnings Exact identifier application number: M020 H.E.B BANANA SPF 50 SUNSCREEN H.E.B b9a9837a-094b-4a57-a50c-5c1437deda7b 2024-10-15 Warnings Exact identifier application number: M020 HEB Solutions Sunscreen SPORT SPF 100 LOTION H.E.B 9e3ea66c-d6a0-49ca-a3c0-8175e0617453 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 LOTION H.E.B 12c76c72-4411-48d5-b79b-c58703bf1fdd 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 50 CONTINUOUS SPRAY H.E.B 86ad5d30-f700-42a2-b810-dd2e3ed0f2d8 2024-10-15 Warnings Exact identifier application number: M020 H.E.B SPF 50 SUNSCREEN H.E.B 1f8d4f91-9eb9-41de-9066-a7a08c7ff84f 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 100 CONTINUOUS SPRAY H.E.B be80244d-da6d-4d37-b228-4d3fac335caf 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen KIDS SPF 50 LOTION SPRAY H.E.B 9b43c5d5-c279-4ae3-843e-1451f7324216 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 2e183ba8-1b83-4211-bc08-dbdcee942ce9 2024-10-15 Warnings Exact identifier application number: M020 EQUALINE KIDS SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE United Natural Foods, Inc. dba UNFI e46cb6e3-ea8d-3c2d-e053-2a95a90a0bf6 2024-10-15 Warnings Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE SUNSCREEN Bentley Laboratories LLC 782a8641-7e6a-413b-a2ed-0efeb36c48a7 2024-10-15 Warnings Exact identifier application number: M020 H.E.B MANGO SPF 50 SUNSCREEN H.E.B 35898f07-2973-461a-91b8-095aa4cf38ee 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen SPORT SPF 30 CONTINUOUS SPRAY H.E.B 8b6d0c0d-485b-4428-91e5-5befcac18d5d 2024-10-15 Warnings Exact identifier application number: M020 H.E.B Solutions Sunscreen ULTRA SPF 50 CONTINUOUS SPRAY H.E.B 5fd3d730-d916-48f4-bb94-62d40d181280 2024-10-15 Warnings 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 49404-153-01 49404015301 1 TUBE in 1 CARTON (49404-153-01) / 50 mL in 1 TUBE 1 tube 2022-12-22 0000-00-00 No No Current 49404-153-02 49404015302 5 mL in 1 TUBE (49404-153-02) 5 ml 2022-12-22 0000-00-00 No No Current