NDC 53138-3012 - Bamboo Mens Thickening
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 53138-3012
- Package NDCs from labels
- 53138-3012-1, 53138-3012-2
- Manufacturer
- Cosway Company, Inc.
- Effective date
- 2011-10-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | Cosway Company, Inc. | 2011-10-19 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53138-3012-2 | 2019-11-13 | C162847 | 48780-1 | 97449f38-ba86-f6ea-e053-dbdaa90aa703 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53138-3012-1 | Bamboo Mens Thickening | 75 mL in 1 TUBE | EMULSION | 75 | 30122 | |
| 53138-3012-2 | Bamboo Mens Thickening | 12 in 1 BOX | EMULSION | 12 | 30122 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 53138-3012 | BAMBOO MENS THICKENING (OCTINOXATE, OCTISALATE) EMULSION [COSWAY COMPANY, INC.] | 30122 | 2 package rows | 20111020_03265d2a-cb6b-432d-ac15-e9cf3da65a80.zip |
DailyMed Socrata Ingredients#
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.
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| Mental Stimulator Formula 2071 | MENTAL STIMULATOR FORMULA | Professional Complementary Health Formulas | b8bbb64c-66f7-457e-88ff-396e374952da | 2026-01-08 | Warnings | CUQ3A77YXI |
| High Energy Ginseng Liquescence 3032 | HIGH ENERGY GINSENG LIQUESCENCE | Professional Complementary Health Formulas | 7b3497bd-3109-4e28-bde9-9b4a8a42eaad | 2026-01-08 | Warnings | CUQ3A77YXI |
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| Pancreas/Stomach Drops 5021 | PANCREAS/STOMACH DROPS | Professional Complementary Health Formulas | 82d4cb86-8650-4218-9481-2dcbcf12cf61 | 2026-01-08 | Warnings | C5529G5JPQ |
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| Sleep Disorder Drops 2152 | SLEEP DISORDER DROPS | Professional Complementary Health Formulas | 55af88df-8e5a-4e84-a8f6-fc3063d91381 | 2026-01-08 | Warnings | CUQ3A77YXI |
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| Circulation Drops 2013 | CIRCULATION DROPS | Professional Complementary Health Formulas | 377f4a5b-bcbb-47b7-b4f4-d198b98c8427 | 2026-01-08 | Warnings | C5529G5JPQ |
| Pain Formula Drops 2046 | PAIN FORMULA DROPS | Professional Complementary Health Formulas | 4456c022-5aac-49b4-b976-b629525f3d49 | 2026-01-08 | Warnings | C5529G5JPQ |
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| CENTELLA RELIEF SOOTHING SUNSCREEN | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | IUNIK Co., Ltd. | 47d170e3-dd76-d413-e063-6294a90ae8e4 | 2026-01-07 | Warnings | 4X49Y0596W |
| Proactiv Clear Skin SPF 30 | AVOBENZONE, OCTISALATE, AND OCTOCRYLENE | Alchemee, LLC | b0aa7ff0-f712-486f-aaaf-f88fed3b5cd1 | 2026-01-07 | Warnings | 4X49Y0596W |
| SHISEIDO SYNCHRO SKIN LASTING Liquid FOUNDATION Neutral 5 | OCTINOXATE AND TITANIUM DIOXIDE | SHISEIDO AMERICAS CORPORATION | 66c22f17-5418-42ff-97b2-33fa10f5eac3 | 2026-01-06 | Warnings | 4Y5P7MUD51 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.