Rx Act Sore Throat description, usages, side effects, indications, overdosage, supplying and lots more!

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Rx Act Sore Throat

H E B

HEB Sore Throat Spray Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Phenol 1.4%

Purpose

Oral anesthetic/analgesic

Rx Act Sore Throat Uses

temporarily relieves sore throat pain, sore mouth, pain associated with canker sores, minor mouth irritation

Warnings

Sore throat warning: Severe or persistent sore throat or sore throat accompanied by fever, headache, rash, swelling, nausea, or vomiting may be serious. Ask a doctor right away. Do not use more than 2 days or give to children under 3 years of age.

When using this product

do not use more than directed

Stop use and ask a doctor if

  • sore mouth symptoms do not improve in 7 days
  • irritation, pain, or redness persists or worsens
  • swelling, rash or fever develops
  • difficulty in breathing occurs

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply to the affected area
  • allow to remain in place for at least 15 seconds, then spit out
  • use every 2 hours or as directed by a doctor or dentist
adults and children 12 years of age & older spray 5 times for each application
children 3 to under 12 years (with adult supervision) spray 3 times for each application
children under 3 years of age ask a doctor or dentist

Other information

store at 20°-25°C (68°-77°F)

Inactive ingredients

D&C green no. 5, D&C yellow no. 10, FD&C green no. 3, flavor, glycerin, purified water, saccharin sodium

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Chloraseptic® active ingredient

SORE THROAT SPRAY

Menthol

Phenol

Oral Anesthetic

Relieves Sore Throat

Instant Acting

GLUTEN FREE

Rx Act Sore Throat
Sore Throat Spray Label

Rx Act Sore Throat

Phenol SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37808-343
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHENOL 1.4 mL

Inactive Ingredients

Ingredient Name Strength
D&C GREEN NO. 5
D&C YELLOW NO. 10
FD&C GREEN NO. 3
GLYCERIN
water
saccharin sodium

Product Characteristics

Color
GREEN (olive;clear)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37808-343-30 177 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 1994-10-25


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Be sure to consult your doctor before taking any medication!
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