Label: ACTIVESSENCE CARIBBEAN COCONUT- alcohol spray
ACTIVESSENCE MARSHMALLOW CLOUD- alcohol spray
ACTIVESSENCE TAHITIAN VANILLA- alcohol spray
ACTIVESSENCE WILD MELON- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 74445-625-01, 74445-626-01, 74445-630-01, 74445-631-01 - Packager: INSTYLE PRODUCTS LLC.
- 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 April 7, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Other Information
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label - Caribbean Coconut
- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label - Marshmallow Cloud
- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label - Tahitian Vanilla
- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label - Wild Melon
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INGREDIENTS AND APPEARANCE
ACTIVESSENCE CARIBBEAN COCONUT
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74445-630 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) PEG-50 Shea Butter (UNII: SF35CE4XLR) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74445-630-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2021 ACTIVESSENCE MARSHMALLOW CLOUD
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74445-631 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) PEG-50 Shea Butter (UNII: SF35CE4XLR) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74445-631-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2021 ACTIVESSENCE TAHITIAN VANILLA
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74445-625 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) PEG-50 Shea Butter (UNII: SF35CE4XLR) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74445-625-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2021 ACTIVESSENCE WILD MELON
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74445-626 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) PEG-50 Shea Butter (UNII: SF35CE4XLR) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74445-626-01 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2021 Labeler - INSTYLE PRODUCTS LLC. (079211341)
