Wild Horse 777 Moisturizing Nasal Spray

Manufacturer
Wild Horse 777, Inc.
Effective date
2022-03-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:48:44

Label at a glance#

ProductWild Horse 777 Moisturizing Nasal
Active ingredientSODIUM CHLORIDE
Label structure8 sections

Indications and uses

- Relieves symptoms of dry, irritated nose. - promotes nasal health. - Clears and invigorates breathing.

Dosage and administration

- 12 years old - adult:3 sprays in each nostril. - 6-12 years old: 2 sprays in each nostril. - 2-6 years old: 1 spray in each nostril. - Children under age 2:1 spray. Consult a physician. - User should be in an upright position. - Remove cap, insert the nozzle into the nostril and depress the pump completely while sniffing deeply. - Day 1: every 3-4 hours. - Day 2: every 3-4 hours. - Day 3: twice a day. - Day 4: a...

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride 0.65%

Purpose:

OTC - PURPOSE SECTION

Moisturizer

Uses

INDICATIONS & USAGE SECTION

- Relieves symptoms of dry, irritated nose.

- promotes nasal health.

- Clears and invigorates breathing.

Warnings

WARNINGS SECTION

- Use only as directed. 

- The use of this container by more than one person may spread infection.

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

consult a health care professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Stop use and ask a doctor

OTC - STOP USE SECTION

- if you experience any discomfort while using this product.

- In case of overdose, get medical help or contact a Poison Control Center at 1-800-222-1222 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

- 12 years old - adult:3 sprays in each nostril.

- 6-12 years old: 2 sprays in each nostril.

- 2-6 years old: 1 spray in each nostril.

- Children under age 2:1 spray. Consult a physician.

- User should be in an upright position.

- Remove cap, insert the nozzle into the nostril and depress the pump completely while sniffing deeply.

- Day 1: every 3-4 hours.

- Day 2: every 3-4 hours.

- Day 3: twice a day.

- Day 4: at bedtime.

- Day 5: at bedtime.

- Day 6-9: skip.

- Day 10: at bedtime (final dose).

Other Information

SPL UNCLASSIFIED SECTION

- Store and use at room temperature.

- Inspect the bottle for integrity. 

- Do not use if the safety seal is torn or broken.

Inactive Ingredient:

INACTIVE INGREDIENT SECTION

Purified mineral water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

15 ml15 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
707251sodium chloride 0.65 % Nasal SprayPSN3
707251sodium chloride 6.5 MG/ML Nasal SpraySCD3
707251NaCl 6.5 MG/ML Nasal SpraySY3
707251sodium chloride 0.65 % Nasal SpraySY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80771-000-15Wild Horse 777 Moisturizing Nasal15 mL in 1 BOTTLELIQUID153
80771-000-15Wild Horse 777 Moisturizing Nasal1 in 1 BOXLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80771-000WILD HORSE 777 MOISTURIZING NASAL (SODIUM CHLORIDE) LIQUID [WILD HORSE 777, INC.]3Current NDC, Legacy NDC, 2 package rows20220315_b0b4dadd-11fa-3dbb-e053-2995a90a2097.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80771-00080771-000-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Wild Horse 777 Moisturizing NasalSODIUM CHLORIDEWild Horse 777, Inc.b0b4dadd-11fa-3dbb-e053-2995a90a20972022-03-14WarningsExact identifier
ndc (package): 80771-000-15
ndc (product): 80771-000
ndc11 (package): 80771000015
spl id: da307e45-06b6-cf3d-e053-2995a90ab8cf
spl set id: b0b4dadd-11fa-3dbb-e053-2995a90a2097

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.