Country: Amerika Syarikat
Bahasa: Inggeris
Sumber: NLM (National Library of Medicine)
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056), MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)
Chattem, Inc.
TOPICAL
OTC DRUG
Anti-itch Anti-itch for temporary relief of pain and itching associated with: ■ minor burns ■ sunburn ■ minor cuts ■ scrapes ■ insect bites ■ minor skin irritations
OTC monograph not final
GOLD BOND INTENSIVE RELIEF ANTI-ITCH- PRAMOXINE HYDROCHLORIDE, MENTHOL LOTION CHATTEM, INC. ---------- GOLD BOND INTENSIVE RELIEF ANTI-ITCH _GOLD BOND® MEDICATED_ _INTENSIVE RELIEF ANTI-ITCH LOTION_ _DRUG FACTS_ _ACTIVE INGREDIENTS_ Menthol 0.5% Pramoxine hydrochloride 1% _PURPOSE_ Anti-itch Anti-itch _USE_ for temporary relief of pain and itching associated with: ■ minor burns ■ sunburn ■ minor cuts ■ scrapes ■ insect bites ■ minor skin irritations _WARNINGS_ FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT ■ avoid contact with eyes STOP USE AND ASK A DOCTOR IF ■ condition worsens ■ symptoms persist for more than 7 days or clear up and occur again within a few days KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center immediately. _DIRECTIONS_ ADULTS AND CHILDREN 2 YEARS OF AGE AND OLDER: apply freely to affected area not more than 3 to 4 times daily CHILDREN UNDER 2 YEARS OF AGE: consult a doctor _INACTIVE INGREDIENTS_ water, glycerin, dimethicone, cetyl alcohol, petrolatum, distearyldimonium chloride, aloe barbadensis leaf juice, glyceryl stearate, stearyl alcohol, cetearyl alcohol, behentrimonium methosulfate, steareth-21, propylene glycol, polysorbate 60, stearamidopropyl PG-dimonium chloride phosphate, diazolidinyl urea, butylene glycol, tocopheryl acetate, potassium hydroxide, methylparaben, panthenol, ethoxydiglycol, EDTA, avena sativa (oat) kernel extract PRINCIPAL DISPLAY PANEL GOLD BOND ANTI-ITCH LOTION INTENSIVE RELIEF Net wt 5.5 oz (155 g) GOLD BOND INTENSIVE RELIEF ANTI-ITCH pramoxine hydrochloride, menthol lotion PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:41167-0507 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 1 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.5 g in 100 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: Baca dokumen lengkap