NDC 70677-1012-01 - Foster and Thrive Childrens Allergy Relief
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
- 70677-1012
- Requested NDC
- 70677-1012-01
- Package NDCs from labels
- 70677-1012-1, 70677-1012-2, 70677-1012-01
- Manufacturer
- Strategic Sourcing Services LLC | Guardian Drug Company
- Effective date
- 2024-12-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diphenhydramine HCl - Strategic Sourcing Services LLC | Guardian Drug Company | Strategic Sourcing Services LLC | Guardian Drug Company | 2024-12-13 | Human OTC Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70677-1012-1 | Foster and Thrive Childrens Allergy Relief | 118 mL in 1 BOTTLE | LIQUID | 118 | 2 | |
| 70677-1012-1 | Foster and Thrive Childrens Allergy Relief | 1 in 1 CARTON | LIQUID | 1 | 2 | |
| 70677-1012-2 | Foster and Thrive Childrens Allergy Relief | 236 mL in 1 BOTTLE | LIQUID | 236 | 2 | |
| 70677-1012-2 | Foster and Thrive Childrens Allergy Relief | 1 in 1 CARTON | LIQUID | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70677-1012 | FOSTER AND THRIVE CHILDRENS ALLERGY RELIEF (DIPHENHYDRAMINE HCL) LIQUID [STRATEGIC SOURCING SERVICES LLC] | 2 | Current NDC, 4 package rows | 20241215_7eaba464-5cdb-4bd4-b272-38fa108658d5.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70677-1012-1 | ML - Milliliter | 70677-1012 | fe420a73-e4db-487d-acf4-a017a71657e8 | 1 | 2023-08-08 |
| 70677-1012-2 | ML - Milliliter | 70677-1012 | 6dc81fa1-0027-4af2-b9b3-528eaf01c987 | 1 | 2023-08-08 |
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 |
|---|---|---|---|---|---|---|
| Daytime Nighttime Ultra Concentrated | DAYTIME - ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL AND NIGHTTIME - ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | KROGER COMPANY | 2be4a37b-44e1-8a8e-e063-6394a90a26a9 | 2025-04-17 | Warnings | M012 |
| good neighbor pharmacy childrens cold and cough | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE | Amerisource Bergen | cde0fd43-771f-4528-bad2-5727efec5250 | 2025-04-17 | Warnings | M012 |
| MUCUS RELIEF | GUAIFENESIN 400 MG | Pioneer Life Sciences, LLC | 729ab412-f30b-4ad1-9d8f-1a5e1c48b118 | 2025-04-16 | Warnings | M012 |
| Diphenhydramine | DIPHENHYDRAMINE HYDROCHLORIDE | Fresenius Kabi USA, LLC | f4f0c26b-dad0-47a1-a9e7-6558c11254c0 | 2025-04-15 | Warnings, Adverse reactions | TC2D6JAD40 |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | 9382c976-3067-4923-a38f-101d1c481e97 | 2025-04-11 | Warnings | M012 TC2D6JAD40 |
| Daytime Nighttime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE AND PHENYLEPHRINE HCL LIQUID FILLED CAPSULES | Walmart Inc. | 263d31c8-bdc2-a289-e063-6394a90a4aaa | 2025-04-10 | Warnings | M012 |
| Bio Co Enzyme Phase | ACONITICUM ACIDUM, CIS-, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ADRENALINUM, , ALPHA-KETOGLUTARICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, ASCORBICUM ACIDUM, BARIUM OXALSUCCINICUM, BETA VULGARIS, CERIUM OXALICUM, CITRICUM ACIDUM, CYSTEINUM, FUMARICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, MAGNESIUM OROTICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM PHOSPHORICUM, NADIDUM, NATRUM OXALACETICUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PANTOTHENIC ACID, PROTEUS (MORGANI), PULSATILLA (PRATENSIS), PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, | Deseret Biologicals, Inc. | 6edee6eb-0ec9-4d2a-9dc9-dc2a6503a6db | 2025-04-08 | Warnings | XF417D3PSL |
| CVS Wild Cherry Throat Drop | PECTIN | CVS | 31f4b641-e9c0-786e-e063-6394a90aa253 | 2025-04-04 | Warnings | M012 |
| Diphenhydramine hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | 829bbcbf-fb27-4484-aff6-a7e7467670af | 2025-04-03 | Warnings, Adverse reactions | TC2D6JAD40 |
| Nighttime Ultra Concentrated Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE SOFTGELS | WALGREENS | 2be0a699-e6ad-ef56-e063-6394a90aaca5 | 2025-04-03 | Warnings | M012 |
| Sleep Aid | DIPHENHYDRAMINE HCL | QUALITY CHOICE (Chain Drug Marketing Association) | 25f32a1c-0687-45e9-8142-96cf63599090 | 2025-04-03 | Warnings | TC2D6JAD40 |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Fresenius Kabi USA, LLC | 6d1aa0e2-036d-4382-a458-fc0300dba7cb | 2025-04-03 | Warnings, Adverse reactions | TC2D6JAD40 |
| Cough and Congestion | DEXTROMETHORPHAN HBR, GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 44fb27d3-5125-4511-84d2-76555bc46e66 | 2025-04-03 | Warnings | M012 |
| Eye Wash | WATER | CMC Group Inc. | 6158a1f5-a6bc-4a3e-9d1d-0a310d9dc561 | 2025-04-02 | Warnings | 059QF0KO0R |
| Guaifenesin | GUAIFENESIN | KESIN PHARMA CORPORATION | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 2025-04-01 | Warnings | M012 |
| Pharmacys Prescription Vapor Rub | MENTHOL | American Consumer Products Corp | 31aa54d8-df8d-f1ae-e063-6294a90a9622 | 2025-03-31 | Warnings | M012 |
| Guaifenesin | GUAIFENESIN | Bryant Ranch Prepack | 570a71eb-2d19-4c7b-8c00-e1524bfa3844 | 2025-03-31 | Warnings | M012 |
| SODIUM PHENYLACETATE and SODIUM BENZOATE | SODIUM PHENYLACETATE AND SODIUM BENZOATE | Ailex Pharmaceuticals, LLC | 329655ae-c3c0-46b2-a925-e49777f2076b | 2025-03-30 | Warnings, Adverse reactions | OJ245FE5EU |
| Sleep Aid | DIPHENHYDRAMINE HCL | FSA Store Inc. (Caring Mills) | 9d32a3a1-9528-4de4-9fd1-1d01a1ad93e9 | 2025-03-28 | Warnings | TC2D6JAD40 |
| Guaifenesin | GUAIFENESIN | KESIN PHARMA CORPORATION | 365c01b7-a197-4876-85fc-42204f787e3a | 2025-03-28 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.