NDC 76348-418-01 - Gold Mountain Beauty Intensive Repair Serum
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
- 76348-418
- Requested NDC
- 76348-418-01
- Package NDCs from labels
- 76348-418-01, 76348-418-02
- Manufacturer
- Renu Laboratories, Inc.
- Effective date
- 2022-01-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GOLD MOUNTAIN BEAUTY FOOT THERAPY INTENSIVE REPAIR SERUM | Renu Laboratories, Inc. | 2022-01-14 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76348-418-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1dca-111a-e063-dadaa90a10e2 | GOLD MOUNTAIN BEAUTY FOOT THERAPY INTENSIVE REPAIR SERUM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76348-418-01 | Gold Mountain Beauty Intensive Repair Serum | 28 g in 1 BOTTLE, PLASTIC | LOTION | 28 | 3 | |
| 76348-418-02 | Gold Mountain Beauty Intensive Repair Serum | 1 in 1 BOX | LOTION | 1 | 3 |
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.
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| Easment DMSO cream | MENTHOL 1.00% | Easment LLC | 48f5544e-1cfd-864a-e063-6394a90a71f1 | 2026-01-22 | Warnings | L7T10EIP3A |
| RAYO ACTIVE ICE | MENTHOL, CAMPHOR | Quimicas Handal de Centroamerica SA de CV | 09e4a36b-020a-c5b1-e063-6394a90a3e31 | 2026-01-22 | Warnings | L7T10EIP3A |
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| ULTRA RELIEF | MENTHOL, CAMPHOR | CHEMCO CORPORATION | 48ea80cf-af54-ce5f-e063-6394a90ac493 | 2026-01-21 | Warnings | L7T10EIP3A |
| Healthy Back Institute Rub On Relief | ANALGESIC | Eagle Labs Inc. | 17dff3c1-3c0b-16f6-e063-6394a90a3c05 | 2026-01-21 | Warnings | L7T10EIP3A |
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| Tolnaftate | FOOT ODOR CONTROL POWDER SPRAY | Meijer Distribution Inc | b3ba676e-9377-4665-b99e-d4143df96b36 | 2026-01-20 | Warnings | 06KB629TKV |
| Tolnaftate | MEIJER ATHLETES FOOT LIQUID | Meijer Distribution Inc. | 0399dfef-9ea6-6fe4-e063-6394a90aec43 | 2026-01-20 | Warnings | 06KB629TKV |
| TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid | TOLNAFTATE | Shenzhen Ctrip Technology Co., Ltd. | 1fb03184-5f21-c82a-e063-6294a90a9fa4 | 2026-01-19 | Warnings | 06KB629TKV |
| SIMPLY VITAL PAIN RELIEF HEMP | MENTHOL | ALPHA PLANTS INC | c14f4c06-cfe5-497e-9f9e-b2ba442e61bb | 2026-01-19 | Warnings | L7T10EIP3A |
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| AsperFlex | MENTHOL AND METHYL SALICYLATE | Akron Pharma Inc. | 117de175-976d-44f3-85ed-3d127fbe3a7c | 2026-01-19 | Warnings | L7T10EIP3A |
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| Hydroseptine | ZINC OXIDE, MENTHOL | AKRON PHARMA INC | 5359d92e-641e-4076-9d91-18daee58a30e | 2026-01-19 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.