Label: CLEARLIFE EXTRA STRENGTH- onion, galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, sulfur, ambrosia artemisiifolia whole, euphrasia stricta and schoenocaulon officinale seed spray
- NDC Code(s): 62795-4006-9
- Packager: MediNatura 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 March 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
-
WARNINGS
Ask a doctor before use if you have asthma. In rare cases broncho-spasm may occur in asthmatic patients. Temporary burning, stinging, sneezing or increased nasal discharge may occur. If pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children. The use of this dispenser by more than one person may spread infection. If symptoms persist or worsen, a healthcare professional should be consulted. Do not use if known sensitivity to ClearLife™ or any of its ingredients exists.
-
Directions:
Adults and children 12 years and older: During an allergy attack: 2 sprays into each nostril every 2-4 hours. For daily protection:2 sprays into each nostril daily. Do not exceed 24 sprays in each nostril per 24 hours.
Children 4 to 11 years: During an allergy attack:1 spray into each nostril every 2 to 4 hours. For daily protection 1 spray into each nostril daily. Do not exceed 12 sprays in each nostril per 24 hours.For children under 4 years, consult your health professional.
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEARLIFE EXTRA STRENGTH
onion, galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, sulfur, ambrosia artemisiifolia whole, euphrasia stricta and schoenocaulon officinale seed sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-4006 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 4 [hp_X] in 20 mL GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E) GALPHIMIA GLAUCA FLOWERING TOP 4 [hp_X] in 20 mL HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 8 [hp_X] in 20 mL LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU) LUFFA OPERCULATA FRUIT 3 [hp_X] in 20 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 4 [hp_X] in 20 mL AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA WHOLE 4 [hp_X] in 20 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 4 [hp_X] in 20 mL SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 4 [hp_X] in 20 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T) SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-4006-9 1 in 1 CARTON 01/06/2021 1 20 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/06/2021 Labeler - MediNatura Inc. (079324099) Establishment Name Address ID/FEI Business Operations MediNatura Inc 102783016 manufacture(62795-4006)
