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United States · US · US:70729-002_e7bbd188-5e3e-4f1c-96d8-53f6de4b3120
Dye Free Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBreeden Brothers, LLC
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11707290022424 TABLET in 1 BOTTLE (70729-002-24)
- ndc11707290025050 TABLET in 1 BOTTLE (70729-002-50)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075139
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WK2XYI10QM",
"rxcui": "5640",
"inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
"display_name": "IBUPROFEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"46846abe-062d-a11f-e063-6294a90a73f3": {
"match": "brand_token",
"title": "DYE FREE REGULAR STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) SUSPENSION [WALMART INC.]",
"spl_version": "2",
"published_date": "2026-02-26"
}
},
"productid": "70729-002_e7bbd188-5e3e-4f1c-96d8-53f6de4b3120",
"productndc": "70729-002",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075139",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 1, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Dye Free Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075139",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "19990301",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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