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United States · US · US:69452-302_3bcb3a5c-d8b2-33eb-e063-6394a90a67ec
dye-free pain relief
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBionpharma Inc.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116945230225180 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-302-25)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A078682
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": {
"48744daa-7079-283d-e063-6394a90a2c9a": {
"match": "brand_token",
"title": "DYE-FREE LORATADINE (LORATADINE) TABLET, CHEWABLE [OHM LABORATORIES INC.]",
"spl_version": "2",
"published_date": "2026-05-21"
}
},
"productid": "69452-302_3bcb3a5c-d8b2-33eb-e063-6394a90a67ec",
"productndc": "69452-302",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "078682",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
"product_no": "001",
"approval_date": "Mar 24, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "dye-free pain relief",
"active_ingred_unit": "mg/1201",
"application_number": "ANDA078682",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20210305",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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