Home NDC 47682-170-33 Green Guard Maximum Strength Non-Aspirin
Product NDC 47682-170
Requested package NDC 47682-170-33
11-digit product format 476820170
Labeler code 47682
Product ID 47682-170_3e4cbfac-83b3-bda3-e063-6294a90a9abd
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Unifirst First Aid Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-02-01
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base Green Guard Maximum Strength Non-Aspirin
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 47682-170-33 Green Guard Maximum Strength Non-Aspirin 50 in 1 BOX TABLET 50 5 47682-170-48 Green Guard Maximum Strength Non-Aspirin 125 in 1 BOX TABLET 125 5 47682-170-99 Green Guard Maximum Strength Non-Aspirin 2 in 1 PACKET TABLET 2 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT O7TSZ97GEP MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 POLYETHYLENE GLYCOL INACTIVE INGREDIENT 3WJQ0SDW1A MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP MEDI-FIRST SINUS DECONGESTANT (PHENYLEPHRINE HYDROCHLORIDE) TABLET, COATED [UNIFIRST FIRST AID CORPORATION] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 47682-170 GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN (ACETAMINOPHEN) TABLET GREEN GUARD MAXIMUM STRENGTH NON-ASPIRIN (ACETAMINOPHEN) TABLET, FILM COATED [UNIFIRST FIRST AID CORPORATION] 4 Current NDC, Legacy NDC, 3 package rows 20250210_f77c9554-d1c2-1682-e053-6294a90ac572.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 85 · 1,681 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 47682-170-33 47682017033 50 PACKET in 1 BOX (47682-170-33) / 2 TABLET in 1 PACKET (47682-170-99) 50 packet 2023-02-01 No No Current