NDC 70994-118 - Everyday Essential Travel Salves 4pc Kit
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
- 70994-118
- Manufacturer
- Sierra Sage Herbs LLC
- Effective date
- 2022-03-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Everyday Essential Travel Salves 4pc Kit - Sierra Sage Herbs LLC | Sierra Sage Herbs LLC | 2022-03-10 | HUMAN OTC DRUG LABEL |
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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| Redicare Cough Drops Cherry Flavored | CHERRY FLAVORED MENTHOL COUGH DROPS | Redicare LLC | 2efeaafa-ee96-37ee-e063-6394a90a9a4b | 2025-02-25 | Warnings | L7T10EIP3A |
| Arnica 30 | ARNCIA 30 | Uriel Pharmacy, Inc | 2eade2a6-a5d6-24a9-e063-6394a90a30ea | 2025-02-21 | Warnings | OZ0E5Y15PZ |
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| CANNA NUMB Roll On | LIDOCAINE HYDROCHLORIDE, MENTHOL | Cannanumb LLC | c1eb0348-3b0e-4f1c-a46b-1ff4aa165fb4 | 2025-02-17 | Warnings | L7T10EIP3A |
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| Halls Sugar Free Cherry | MENTHOL | Mondelez Global LLC | ea8dfe96-f6a4-4172-bf9e-ae3cf606ff50 | 2025-02-14 | Warnings | L7T10EIP3A |
| Halls Sugar Free Watermelon | MENTHOL | Mondelez Global LLC | c4c090ca-f083-74e0-e053-2a95a90a9d60 | 2025-02-14 | Warnings | L7T10EIP3A |
| Vaporizing Chest Rub 4 oz. | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Rejoice International Inc. | 7173b141-123e-6cd4-e053-2a95a90a8600 | 2025-02-12 | Warnings | L7T10EIP3A |
| Vaporizing Chest Rub 4 oz. 3 pk | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Rejoice International Inc. | 71c186a1-8283-2482-e053-2995a90acc1f | 2025-02-12 | Warnings | L7T10EIP3A |
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy, Inc | 2df4f968-af1d-82f1-e063-6294a90a65be | 2025-02-12 | Warnings | UFH8805FKA |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.