FDA.reportPublic FDA data

Green Guard Ibuprofen Relief

Product NDC
47682-710
11-digit product format
476820710
Labeler code
47682
Product ID
47682-710_3e5d4984-a2e9-a9fc-e063-6394a90a4396
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Unifirst First Aid
Application
ANDA079174
Marketing category
ANDA
Marketing start
2017-01-26
Substance
IBUPROFEN
Active strength
200 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Green Guard Ibuprofen Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui310965

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-710-33Green Guard Ibuprofen Relief50 in 1 BOXTABLET, COATED5015
47682-710-48Green Guard Ibuprofen Relief125 in 1 BOXTABLET, COATED12515
47682-710-48Green Guard Ibuprofen Relief2 in 1 PACKETTABLET, COATED215
47682-710-99Green Guard Ibuprofen Relief2 in 1 PACKETTABLET, COATED215

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IBUPROFENACTIVE INGREDIENTWK2XYI10QMGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
IBUPROFENACTIVE MOIETYWK2XYI10QMGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675GREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
POVIDONE K30INACTIVE INGREDIENTU725QWY32XGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4GREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2GREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPGREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1
TRIACETININACTIVE INGREDIENTXHX3C3X673GREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47682-710GREEN GUARD IBUPROFEN RELIEF (IBUPROFEN) TABLET, COATED [UNIFIRST FIRST AID]14Current NDC, Legacy NDC, 4 package rows20250210_0798e401-8247-2fce-e054-00144ff8d46c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN0798e401-8247-2fce-e054-00144ff8d46c15
310965ibuprofen 200 MG Oral TabletSCD0798e401-8247-2fce-e054-00144ff8d46c15
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY0798e401-8247-2fce-e054-00144ff8d46c15

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
47682-710-334768207103350 PACKET in 1 BOX (47682-710-33) / 2 TABLET, COATED in 1 PACKET (47682-710-99) 50 packet2017-01-260000-00-00NoNoCurrent
47682-710-4847682071048125 PACKET in 1 BOX (47682-710-48) / 2 TABLET, COATED in 1 PACKET125 packet2017-01-260000-00-00NoNoCurrent
47682-710-99476820710992 TABLET, COATED in 1 PACKET (47682-710-99) 2017-01-26NoNoHistorical