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United States · US · US:13709-315_0eb0265b-79a8-8489-e063-6394a90a1967
No Drip
UNIISPLATC D11AX27
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNeilMed Pharmaceuticals Inc
CountryUS (United States)
ATC codeD11AX27
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1113709315011 BOTTLE, SPRAY in 1 CARTON (13709-315-01) / 30 mL in 1 BOTTLE, SPRAY
Annotations
UNII (FDA Substance ID)
K89MJ0S5VY
OXYMETAZOLINE HYDROCHLORIDE
RxCUI 106101
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "K89MJ0S5VY",
"rxcui": "106101",
"inchikey": "BEEDODBODQVSIM-UHFFFAOYSA-N",
"display_name": "OXYMETAZOLINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "NASAL",
"spl_meta": {
"50b3e9fa-faf8-0026-e063-6294a90a0823": {
"match": "brand_token",
"title": "NO 7 PRIME FOREVER SPF 50 PRIMER (NO 7 PRIME FOREVER BROAD SPECTRUM SUNSCREEN SPF50 PRIMER) LOTION [BOOTS RETAIL USA]",
"spl_version": "1",
"published_date": "2026-05-07"
}
},
"productid": "13709-315_0eb0265b-79a8-8489-e063-6394a90a1967",
"productndc": "13709-315",
"dosage_form": "SPRAY",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OXYMETAZOLINE HYDROCHLORIDE",
"proprietary_name": "No Drip",
"active_ingred_unit": "mg/30mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Oxymetazoline Hydrochloride",
"start_marketing_date": "20221001",
"active_numerator_strength": "15"
}Related drugs
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