Label: BIOSILK GARDENIA- alcohol spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 73740-3031-2 - Packager: Farouk Systems, Inc.
- 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 8, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Stop use and ask a doctor
- Active ingredient
- Stop use and ask a doctor
- Stop use and ask a doctor
- Keep out of reach of children.
- Use[s]
- Directions
- Inactive ingredients:
-
Warnings
Warnings
Flammable. Keep away from fire and
flames.
For external use only.
When using this product
do not get into eyes
if contact occurs, rinse eyes
thoroughly with water
Stop use and ask a
doctor if irritation and
redness develop
Keep out of reach of
children. If
swallowed, get
medical help or
contact a Poison
Control Center
right away.
- Use[s]
- BioSilk Health Beauty Moisturizing Sanitizer Spray with Aloe Vera & Gardenia
-
INGREDIENTS AND APPEARANCE
BIOSILK GARDENIA
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73740-3031 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 g in 100 g Inactive Ingredients Ingredient Name Strength FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0) 0.117225 g in 100 g ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.001 g in 100 g BENZYL BENZOATE (UNII: N863NB338G) 0.1295 g in 100 g EUGENOL (UNII: 3T8H1794QW) 0.001075 g in 100 g HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) 0.001175 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 2 g in 100 g BENZYL SALICYLATE (UNII: WAO5MNK9TU) 0.001025 g in 100 g WATER (UNII: 059QF0KO0R) 22.749 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73740-3031-2 65 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 10/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/08/2020 Labeler - Farouk Systems, Inc. (137598132) Registrant - Farouk Systems, Inc. (137598132) Establishment Name Address ID/FEI Business Operations Farouk Systems, Inc. 137598132 manufacture(73740-3031)