Label: WALMART SALINE (saline nasal- sodium chloride spray
- NDC Code(s): 79903-304-30
- Packager: WALMART STORES INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 15, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
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INDICATIONS & USAGE
Uses
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- Moisturizes dry, irritated, or crusty nasal passages due to low humidity, heated environments, air travel, allergies or colds.
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- Helps loosens mucus secretions to aid aspiration and removal from nose and sinuses allowing for easier breathing. For newborns/infant this can be assisted with the use of our specially soft tip nasal Aspirator
Warnings
Directions (For nasal use only)
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- Newborns/ Infants- 2 to 6 drops in each nostril as often as needed or as directed by your doctor.
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- Children & Adults -2 to 6 Sprays /drops into each nostril as often as needed or as directed by a doctor.
Other Information
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- This product is non-medicated and can be used as often as needed without the worry of any harmful side effects or drug interactions. The specially buffered formula is alcohol free and helps moisturize nasal membranes. Works on adult too!
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- Store at room temperature
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- See bottle or box for Lot No. and Exp. Date
- Warnings
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
NDC 79903-304-30
SAFE FOR NEWBORNS
SALINE SPRAY + DROPS
Beathe Easy
Gently Wash Away Mucus
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- No Artificial Flavors
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- No Artificial Dyes
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- No Parabens
1 FL OZ (30 mL)
To use as a dropper:
Hold bottle upside down and squeeze lightly.
To use as a gentle sprayer:
Hold bottle upright and squeeze firm.
DO NOT USE IF IMPRINTED PLASTIC NECKBAND IS BROKEN OR MISSING
Distributed by:
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INGREDIENTS AND APPEARANCE
WALMART SALINE
saline nasal (sodium chloride) sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-304 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 6.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74) SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU) BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-304-30 1 in 1 CARTON 09/27/2024 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 09/27/2024 Labeler - WALMART STORES INC (051957769)