NDC 84994-002-01 - Practical Alchemy Purify and Protect Duo
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
- 84994-002
- Requested NDC
- 84994-002-01
- Package NDCs from labels
- 84994-002-01, 84994-002-15
- Manufacturer
- Over Here, LLC | A.I.G. TECHNOLOGIES, INC. | JP Packaging LLC
- Effective date
- 2025-04-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Practical Alchemy - Purify + Protect Duo - Dual Sachet | Over Here, LLC | A.I.G. TECHNOLOGIES, INC. | JP Packaging LLC | 2025-04-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84994-001-01 | Practical Alchemy Purify and Protect Duo | 1.5 g in 1 PACKET | CREAM | 1.5 g | 14.6 g in 100g | 5 |
| 84994-002-01 | Practical Alchemy Purify and Protect Duo | 1 in 1 PACKAGE, COMBINATION | KIT | 1 | 5 | |
| 84994-002-15 | Practical Alchemy Purify and Protect Duo | 15 in 1 CARTON | KIT | 15 | 5 |
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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| NATURIUM Dew-Glow Moisturizer SPF 50 | NATURIUM DEW-GLOW MOISTURIZER SPF 50 | PML NYC, LLC | 00c93b11-754e-701c-e063-6294a90a3b1d | 2026-04-14 | Warnings | M020 |
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| MIDHA Rice Daily Moisture Sun Cream | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | MIDHA Cosmetic Co.,Ltd. | 4b394107-7830-c2c6-e063-6294a90a07d9 | 2026-04-10 | Warnings | M020 |
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| Abib Dewy tinted sunscreen Glow tube Light | OCTISALATE, OCTOCRYLENE, ZINC OXIDE | FOURCOMPANY CO., LTD. | 4f165895-aa84-e215-e063-6394a90a6256 | 2026-04-10 | Warnings | M020 SOI2LOH54Z |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.