Home NDC 70677-1276 foster and thrive rapid release pain relief
Product NDC 70677-1276
11-digit product format 706771276
Labeler code 70677
Product ID 70677-1276_18f1208d-053b-4e08-8389-c432ac63e8db
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Strategic Sourcing Services LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-16
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base foster and thrive rapid release pain relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70677-1276-1 foster and thrive rapid release pain relief 225 in 1 BOTTLE TABLET, FILM COATED 225 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-1276 FOSTER AND THRIVE RAPID RELEASE PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [STRATEGIC SOURCING SERVICES LLC] 2 Current NDC, 1 package rows 20250119_d2130173-b107-4ae6-a1f7-6db467da3820.zip
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.
Matched openFDA labels page 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 70677-1276-1 70677127601 225 TABLET, FILM COATED in 1 BOTTLE (70677-1276-1) 2025-01-16 No No Current