Sunscreen
- Product NDC
- 30142-714
- 11-digit product format
- 301420714
- Labeler code
- 30142
- Product ID
- 30142-714_4bd1a6eb-2184-38d5-e063-6294a90a8bcb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- The Kroger Co.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-11-28
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 30142-714-34 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 30142-714-34 | cdf11ea48f46… | ba0047e9e063… |
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
- Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 100 mg/mL |
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 100 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| G63QQF2NOX | Internal UNII lookup |
| V06SV4M95S | Internal UNII lookup |
| 4X49Y0596W | Internal UNII lookup |
| 5A68WGF6WM | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3ae7e275-7bbc-4e62-b30f-013c40a89949 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 9869efd7-d6dd-0665-5b67-53adbe6ef15e | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 30142-714-34 | Sunscreen | 236 mL in 1 BOTTLE, PLASTIC | LOTION | 236 | 29 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Laxomil | BISACODYL 5MG | Pharmadel LLC | 3999935b-d8e8-52a6-e063-6294a90aa2a2 | 2026-03-20 | Warnings | M007 |
| Laxative Enteric Coated | BISACODYL 5MG | Grocery Outlet | c820e6a1-fa23-447a-9ee9-50a1bd617adb | 2026-03-19 | Warnings | M007 |
| CITRUCEL | METHYLCELLULOSE | Haleon US Holdings LLC | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 2026-03-18 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Safeway, Inc. | f178b31d-4843-4b91-a0d5-ab5ade835dc2 | 2026-03-16 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Safeway, Inc. | 12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c | 2026-03-13 | Warnings | M007 |
| Castor Oil | CASTOR OIL | Old East Main Co. | a1ca668a-3bf9-46a9-8a4f-5cb61547bb81 | 2026-03-12 | Warnings, Adverse reactions | M007 |
| Castor Oil | CASTOR OIL | Vi-Jon, LLC | b29775df-8470-4fe3-bee3-f0490ea6903f | 2026-03-12 | Warnings | M007 |
| Castor Oil | CASTOR OIL | Nice-Pak Products, LLC | cc43d514-ee82-4314-99b2-c64380f98779 | 2026-03-12 | Warnings, Adverse reactions | M007 |
| Fibercon | CALCIUM POLYCARBOPHIL | Foundation Consumer Brands | 7992a4bb-5535-4a1d-867d-a99f7e0c1be7 | 2026-03-12 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Walgreens | cda27a9c-9175-4b07-9c0b-d8d897882965 | 2026-03-12 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Lemon Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | aa02c9af-22b8-4ec2-9e43-fe073f5e617b | 2026-03-11 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Grape Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | 021ebb61-2466-4272-8f7d-b49cafd08754 | 2026-03-11 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Cherry Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | 1f14411b-6833-40e6-b1a5-2b8c5bf709d3 | 2026-03-11 | Warnings | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | f83ba007-734d-4910-87cb-02e45285e161 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | 57e914fa-8fa2-4221-bb5f-534f0ea0aba7 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | f28a9043-e0ee-4b38-95d9-d3f23d400691 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Stool Softener | DOCUSATE SODIUM | Amerisource Bergen | 4caf0bcb-c1bf-0ae7-e063-6294a90a344b | 2026-03-10 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Walgreens | 92df761b-da68-4ce9-b02a-a5a74fd6620e | 2026-03-10 | Warnings | M007 |
| Fleet | GLYCERIN | C.B. Fleet Company, Inc. | 31778652-e60e-4098-8e90-3e4f56b5800c | 2026-03-06 | Warnings | M007 |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 4c6094b7-c1ef-26a3-e063-6394a90af4cc | 2026-03-06 | Warnings | M007 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 30142-714-34 | 30142071434 | 236 mL in 1 BOTTLE, PLASTIC (30142-714-34) | 236 ml | 2016-11-28 | 0000-00-00 | No | No | Current |