Ország: Egyesült Államok
Nyelv: angol
Forrás: NLM (National Library of Medicine)
purified water
2359 US INC
VAGINAL
OTC DRUG
Purified Water------------Vaginal Irrigation Vaginal douche for disinfection. pH balance, and skin barrier. Relieves minor vaginal like itching or soreness.
unapproved drug other
PURIFIED WATER- HYALURONIC ACID INJECTION, SOLUTION 2359 US INC _Disclaimer: This drug has not been found by FDA to be safe and effective, and this_ _labeling has not been approved by FDA. For further information about unapproved_ _drugs, click here._ ---------- 83490-315 LACTOMEDI VAGINAL IRRIGATION ACTIVE INGREDIENTS purified water PURPOSES Purified Water------------Vaginal Irrigation USES Vaginal douche for disinfection. pH balance, and skin barrier. Relieves minor vaginal like itching or soreness. WARNINGS Do not use the product to areas with scars, eczema, or dermatitis. WARNINGS If swallowed, get medical help or contact a Poison Control Center immediately. WARNINGS Stop use and ask a doctor if irritation, rash, red spot on the skin, or swelling occurs. These may be signs of a severe condition. WARNINGS When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. WARNINGS This product is for external use only. Women during menstruation and pregnancy should not use it. Not suitable for children under 3 years of age. DIRECTIONS Use the product as a douche as needed. INACTIVE INGREDIENTS HYALURONIC ACID LABEL PURIFIED WATER hyaluronic acid injection, solution PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:83490-315 ROUTE OF ADMINISTRATION VAGINAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 99.99 g in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH HYALURONIC ACID (UNII: S270N0TRQY) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:83490- 315-01 50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 06/01/2023 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE unapproved drug other 06/01/2023 2359 US INC LABELER - 2359 US INC (11897 Olvassa el a teljes dokumentumot