Label: WIPE OUT-LAVENDER SCENT- wipe out spray-lavender scent spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 75606-004-01 - Packager: Xiamen Tesimeier Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 17, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
-
Warnings
For external use only
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- Do not use
-
WHEN USING
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
WIPE OUT-LAVENDER SCENT
wipe out spray-lavender scent sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75606-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) FRAGRANCE LAVENDER ORC1800979 (UNII: 1B40MIN2W5) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75606-004-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Xiamen Tesimeier Biotechnology Co., Ltd. (550462445) Establishment Name Address ID/FEI Business Operations Xiamen Tesimeier Biotechnology Co., Ltd. 550462445 manufacture(75606-004)
