13709-231 : Sinufrin 7.5 mg/15ml Nasal Spray
| NDC: | 13709-231 |
| Labeler: | Neilmed Pharmaceuticals Inc |
| Product Type: | Human OTC Drug |
| Drug Name: |  Sinufrin Neilmed |
| Dosage Form: | Nasal Spray |
| Application #: | part341 |
| Rev. Date: | |
| CSA Schedule: | CII (US) [1] |
[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.
NDC Package Codes:
- 13709-231-04: 15 ML IN 1 BOX (13709‑231‑04)
- 13709-231-07: 15 ML IN 1 BOTTLE (13709‑231‑07)
- 13709-231-12: 1 BOTTLE IN 1 CARTON (13709‑231‑12) > 30 ML IN 1 BOTTLE
Active Ingredients:
- Oxymetazoline Hydrochloride
Dosage Strength:
- 7.5 mg/15mL
Pharmaceutical Classes:
- Imidazolines [CS]
- Increased Sympathetic Activity [PE]
- Vasoconstriction [PE]
- Vasoconstrictor [EPC]
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.