Država: Sjedinjene Američke Države
Jezik: engleski
Izvor: NLM (National Library of Medicine)
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)
P & L Development, LLC
WITCH HAZEL
WITCH HAZEL 86 g in 100 mL
TOPICAL
OTC DRUG
Astringent - for relief of minor skin irritations due to: insect bites minor cuts minor scrapes - insect bites - minor cuts - minor scrapes
OTC monograph final
WITCH HAZEL READYINCASE- WITCH HAZEL LIQUID P & L DEVELOPMENT, LLC ---------- DRUG FACTS ACTIVE INGREDIENT Witch hazel 86% PURPOSE Astringent USES for relief of minor skin irritations due to: insect bites minor cuts minor scrapes WARNINGS FOR EXTERNAL USE ONLY avoid swallowing WHEN USING THIS PRODUCT avoid contact with the eyes. If contact occurs, rinse thoroughly with water. STOP USE AND ASK A DOCTOR IF condition worsens or symptoms persist for more than 7 days. IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. DIRECTIONS apply to the affected area as often as necessary. OTHER INFORMATION keep tightly closed store at room temperature INACTIVE INGREDIENT alcohol 14% by volume PRINCIPAL DISPLAY PANEL Distilled extract of WITCH HAZEL Astringent alcohol 14% by volume hamamelis water for relief of minor skin irritations due to insect bites minor cuts minor scrapes fl oz (PT) mL Manufactured by: PL Developments 1874 Hwy 72 W Clinton, SC 29325 Questions or comments? Call 1-877-753-3935 Monday-Friday 9AM-5PM EST TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING. PACKAGE LABEL READYINCASE WITCH HAZEL WITCH HAZEL READYINCASE witch hazel liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:49580-0390 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 86 g in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ALCOHOL (UNII: 3K9958V90M) P & L Development, LLC PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:49580- 0390-6 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/31/2014 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M016 08/31/2014 LABELER - P Pročitajte cijeli dokument