Label: NETIMIST- homeopathic sinus spray spray
- NDC Code(s): 13709-234-01
- Packager: NeilMed Pharmaceuticals, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Warnings
- Inactive Ingredients
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Directions
- Suitable for children over 6 with proper adult supervision.
- For children 6 and under, consult a physician before use.
- Shake well.
- Remove cap & safety clip.
- Hold with thumb at bottom of bottle & nozzle between fingers.
- Prime pump prior to initial use by depressing several times.
- Insert tip of nozzle, just past the nasal opening (1/8th - 1/4th inch)
- Pump once inside each nostril & gently inhale.
- Wait atleast 30 seconds or longer before blowing nose.
- Use as needed every 2-4 hours & in crowded public environments such as schools, public transpotation.
- Uses
- Keep out of reach of children
- Drug Facts
- Drug Facts
- When using this product:
- Ask a doctor before use if you have:
- Stop Use and ask Doctor if :
- Other Information
- Netimist - Kids
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INGREDIENTS AND APPEARANCE
NETIMIST
homeopathic sinus spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13709-234 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_X] in 30 mL Inactive Ingredients Ingredient Name Strength ALOE SUCCOTRINA WHOLE (UNII: M6U8N4MD5P) TANGERINE (UNII: KH3E3096OO) GRAPEFRUIT SEED OIL (UNII: 598D944HOL) SODIUM BICARBONATE (UNII: 8MDF5V39QO) GINGER OIL (UNII: SAS9Z1SVUK) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13709-234-01 1 in 1 BOX 04/29/2016 1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/29/2016 Labeler - NeilMed Pharmaceuticals, Inc (799295915) Establishment Name Address ID/FEI Business Operations NeilMed Pharmaceuticals, Inc. 799295915 manufacture(13709-234)