Label: SKIN PROTECTANT- astrigent cream
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Contains inactivated NDC Code(s)
NDC Code(s): 35192-029-05 - Packager: CA-Botana International
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 16, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Aluminum acetate 0.2%
- For external use only. Avoid contact with eyes. Do not apply to open wounds. S TOP USE and ask a doctor if condition worsens or symtomps persist for more than seven days. Keep out reach of children
- Directions: Adults and childrens tho years of age and older apply to affected area as needed or as directed by a doctor. Consult a doctor for children under the age of two
- Relieves minor skin irritations due to poison Ivi. Poison oak. Poison sumac. Insect bites Athlete's foot. Allergic itches. Irritations
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INACTIVE INGREDIENT
Cetyl Alcohol, Dimethico 100, Polyacrylic Acid, Polawax Polysorbate, Glycerin, Caprylyl Glycol, Ceramide NG, Water, Magnesium Aluminum Silicate, Glyceryl Stearate, Edenate Disodium, Tocopherol, Tetrahexyldecyl Ascorbate, Shea Butter, Phenoxyethanol, Strontium Nitrate, Xanthan Gum Hyaloronic acid, Stearyl Alcohol, IsopropyylMyrristate, Caprylic/Capric Tryglyceride
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- label
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INGREDIENTS AND APPEARANCE
SKIN PROTECTANT
astrigent creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:35192-029 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE 0.2 g in 30 g Inactive Ingredients Ingredient Name Strength XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CERAMIDE NG (UNII: C04977SRJ5) WATER O-18 (UNII: 7QV8F8BYNJ) MAGNESIUM ALUMINUM SILICATE TYPE IA (UNII: SUS08ZOA9S) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) EDETATE DISODIUM (UNII: 7FLD91C86K) TOCOPHEROL (UNII: R0ZB2556P8) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) SHEA BUTTER (UNII: K49155WL9Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) STRONTIUM NITRATE (UNII: BDG873AQZL) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE 100 (UNII: RO266O364U) POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3) HYALURONIC ACID (UNII: S270N0TRQY) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) POLAWAX POLYSORBATE (UNII: Q504PL8E0V) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:35192-029-05 30 g in 1 TUBE; Type 0: Not a Combination Product 04/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/10/2020 Labeler - CA-Botana International (106276728) Registrant - Rodolfo Ugelstad (106276728) Establishment Name Address ID/FEI Business Operations CA-Botana International 106276728 manufacture(35192-029)
